510(k) Report

510(k) · Cleared

Cleared

Athena GTX Device Management Suite (ADMS) Software

K173203510(k) TraditionalCleared Mar 14, 2018163-day reviewClass II21 CFR 870.2300

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Athena Gtx · MSX System, Network And Communication, Physiological Monitors

Cleared on Mar 14, 2018 as substantially equivalent to K163584 (Philips Medical Systems, 2017) and 1 other predicate after a 163-day review. Its family tree reaches back 26 generations to 1994.

Decided
Mar 14, 2018
Review
163 days
Class
Class II
Product code
MSX
Recalls
None
Predicates
2

Its longest line of descent runs back 26 generations to K941811 (1994). 165 ancestors in all, the oldest K872781 (1987). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2013: 1 other ancestor2010: 1 other ancestor2007: 1 other ancestor2005: 3 other ancestors2004: 11 other ancestors2002: 14 other ancestors2003: 7 other ancestors2001: 6 other ancestors2000: 20 other ancestors1997: 7 other ancestors1996: 8 other ancestors1994: 3 other ancestors1991: 7 other ancestors1999: 10 other ancestors1995: 6 other ancestors1993: 6 other ancestors1998: 13 other ancestors1990: 6 other ancestors1989: 2 other ancestors1992: 6 other ancestors1987: 1 other ancestorK941811 · HP M1175A, M1176A, Component Monitoring System · Hewlett-Packard Co. · 1994K960934 · HP M1205A Omnicare Component Monitor System Model 24 · Hewlett-Packard Co. · 1996×3: 3 generations cleared close together, K981376 (1999), K990125 (1999), K990972 (1999) ×3: 3 generations cleared close together, K013199 (2001), K020531 (2002), K021778 (2002) ×3: 3 generations cleared close together, K023871 (2002), K030038 (2003), K031481 (2003) K032858 · The Philips Intellivue MP40, MP50, MP60, MP70,and MP90 Patient Monitors, Release B.O. · Philips Medizin Systeme Boblingen GmbH · 2003×2: 2 generations cleared close together, K040304 (2004), K041235 (2004) ×6: 6 generations cleared close together, K042845 (2004), K050141 (2005), K050762 (2005), K051106 (2005), K052801 (2005), K053522 (2006) K062271 · M3290A Intellivue Information Center Software, Release J.00 (for M3140, M3145, M3150, M3151, M3154, M3155, M3169, M3170) · Philips Medical Systems · 2006 · recalledK081983 · M3290A Intellivue Information Center Software, Release 1.00 · Philips Medical Systems · 2008 · recalledK102495 · M3290B Intellivue Information Center Software, Release a.0 · Philips Medical Systems · 2010 · recalledK143057 · M3290B Philips IntelliVue Information Center iX · Philips Medical Systems · 2014 · recalledK153702 · M3290B Philips IntelliVue Information Center iX · Philips Medical Systems · 2016 · recalledK163584 · M3290B Philips IntelliVue Information Center iX · Philips Medical Systems · 201719851990199520002005201020152020
Other ancestors, by generation 1 generation back: 1 other ancestor2 generations back: 1 other ancestor3 generations back: 5 other ancestors4 generations back: 10 other ancestors5 generations back: 22 other ancestors6 generations back: 8 other ancestors7 generations back: 22 other ancestors8 generations back: 25 other ancestors9 generations back: 17 other ancestors10 generations back: 7 other ancestors11 generations back: 10 other ancestors12 generations back: 6 other ancestors13 generations back: 5 other ancestors K163584 · M3290B Philips IntelliVue Information Center iX · Philips Medical Systems · 2017K153702 · M3290B Philips IntelliVue Information Center iX · Philips Medical Systems · 2016 · recalledK143057 · M3290B Philips IntelliVue Information Center iX · Philips Medical Systems · 2014 · recalledK102495 · M3290B Intellivue Information Center Software, Release a.0 · Philips Medical Systems · 2010 · recalledK081983 · M3290A Intellivue Information Center Software, Release 1.00 · Philips Medical Systems · 2008 · recalledK062271 · M3290A Intellivue Information Center Software, Release J.00 (for M3140, M3145, M3150, M3151, M3154, M3155, M3169, M3170) · Philips Medical Systems · 2006 · recalledK053522 · Philips MP40, MP50, MP60, MP70, MP80 and MP90 Intellivue Patient Monitors, Release D.00 · Philips Medizin Systeme Boeblingen GmbH · 2006K052801 · Intellivue Patient Monitors with Release C.02, Models MP20, MP30, MP40, MP50, MP60, MP70, MP80 and MP90 · Philips Medizin Systeme Boeblingen GmbH · 2005K051106 · The Philips MP20, MP30, MP40, MP50, MP60, MP70, MP80 and MP90 Intellivue Patient Monitors · Philips Medizin Systeme Boeblingen GmbH · 2005K050762 · Philips Intellivue Patient Monitor, Models MP20, MP30, MP40, MP50, MP60, MP70 and MP90 · Philips Medizin Systeme Boeblingen GmbH · 2005K050141 · The Philips MP20, MP30, MP40, MP50, MP60, MP70 and MP90 Intellivue Patient Monitors · Philips Medizin Systeme Boeblingen GmbH · 2005K042845 · The Philips MP20, MP30, MP40, MP50, MP60, MP70, and MP90 Intellivue Patient Monitors · Philips Medizin Systeme Boblingen GmbH · 2004K041235 · Philips MP20, MP30, MP40, MP50. MP60, MP70 and MP90 Intellivue Patient Monitors · Philips Medizin Systeme Boeblingen GmbH · 2004K040304 · Philips Intellivue Patient Monitor, Models MP40 & MP50 · Philips Medizin Systeme Boeblingen GmbH · 2004K032858 · The Philips Intellivue MP40, MP50, MP60, MP70,and MP90 Patient Monitors, Release B.O. · Philips Medizin Systeme Boblingen GmbH · 2003K031481 · The Philips Intellivue MP60, MP70, and MP90 Patient Monitors, Release a.20 · Philips Medizin Systeme Boblingen GmbH · 2003K030038 · Philips MP60, MP70 and MP90 Intellivue Patient Monitors with Portal Technology and M3185 Opt C41 Wireless Bedside Adaptr · Philips Medical Systems, Inc. · 2003K023871 · M3046A (M2/M3/M4) Compact Portable Patient Monitor and MP60 & MP70 Intellivue Patient Monitor with Portal Technology · Philips Medical Systems · 2002K021778 · Philips Component Compact Monitor, Release a.04, Model #M1275B · Philips Medical Systems · 2002K020531 · Philips Multi-Parameter Module, Model M3001A; Philips Component Compact Monitor, Release a.02, Model M1275B · Philips Medical Systems · 2002K013199 · Philips Component Compact Monitor,Model M1275B, Philips Compenent Rack, Model M1276B · Philips Medical Systems, Inc. · 2001K990972 · HP Viridia Component Monitoring System, HP Viridia CMS 24/26, HP Viridia Multi-Measurement Server and Compact Portable T · Hewlett-Packard GmbH · 1999K990125 · HP Viridia Component Monitoring System, Model Rev. K · Hewlett-Packard GmbH · 1999K981376 · Hewlett-Packard M1205A Viridia 24 CT · Hewlett-Packard Co. · 1999K960934 · HP M1205A Omnicare Component Monitor System Model 24 · Hewlett-Packard Co. · 1996K941811 · HP M1175A, M1176A, Component Monitoring System · Hewlett-Packard Co. · 1994−25−20−15−10−50
  1. Root · 26 generations backK941811 HP M1175A, M1176A, Component Monitoring SystemHewlett-Packard Co. · 1994
  2. 22 generations between
  3. 3 generations backK143057 M3290B Philips IntelliVue Information Center iXPhilips Medical Systems · 2014 · Recalled
  4. 2 generations backK153702 M3290B Philips IntelliVue Information Center iXPhilips Medical Systems · 2016 · Recalled
  5. 1 generation backK163584 M3290B Philips IntelliVue Information Center iXPhilips Medical Systems · 2017
  6. This deviceK173203 Athena GTX Device Management Suite (ADMS) SoftwareAthena Gtx · 2018
Show all 26 generations
  1. Root · 26 generations backK941811 HP M1175A, M1176A, Component Monitoring SystemHewlett-Packard Co. · 1994
  2. 25 generations backK960934 HP M1205A Omnicare Component Monitor System Model 24Hewlett-Packard Co. · 1996
  3. 24 generations backK981376 Hewlett-Packard M1205A Viridia 24 CTHewlett-Packard Co. · 1999
  4. 23 generations backK990125 HP Viridia Component Monitoring System, Model Rev. KHewlett-Packard GmbH · 1999
  5. 22 generations backK990972 HP Viridia Component Monitoring System, HP Viridia CMS 24/26, HP…Hewlett-Packard GmbH · 1999
  6. 21 generations backK013199 Philips Component Compact Monitor,Model M1275B, Philips Compenent…Philips Medical Systems, Inc. · 2001
  7. 20 generations backK020531 Philips Multi-Parameter Module, Model M3001A; Philips Component…Philips Medical Systems · 2002
  8. 19 generations backK021778 Philips Component Compact Monitor, Release a.04, Model #M1275BPhilips Medical Systems · 2002
  9. 18 generations backK023871 M3046A (M2/M3/M4) Compact Portable Patient Monitor and MP60 & MP70…Philips Medical Systems · 2002
  10. 17 generations backK030038 Philips MP60, MP70 and MP90 Intellivue Patient Monitors with Portal…Philips Medical Systems, Inc. · 2003
  11. 16 generations backK031481 The Philips Intellivue MP60, MP70, and MP90 Patient Monitors…Philips Medizin Systeme Boblingen GmbH · 2003
  12. 15 generations backK032858 The Philips Intellivue MP40, MP50, MP60, MP70,and MP90 Patient…Philips Medizin Systeme Boblingen GmbH · 2003
  13. 14 generations backK040304 Philips Intellivue Patient Monitor, Models MP40 & MP50Philips Medizin Systeme Boeblingen GmbH · 2004
  14. 13 generations backK041235 Philips MP20, MP30, MP40, MP50. MP60, MP70 and MP90 Intellivue…Philips Medizin Systeme Boeblingen GmbH · 2004
  15. 12 generations backK042845 The Philips MP20, MP30, MP40, MP50, MP60, MP70, and MP90 Intellivue…Philips Medizin Systeme Boblingen GmbH · 2004
  16. 11 generations backK050141 The Philips MP20, MP30, MP40, MP50, MP60, MP70 and MP90 Intellivue…Philips Medizin Systeme Boeblingen GmbH · 2005
  17. 10 generations backK050762 Philips Intellivue Patient Monitor, Models MP20, MP30, MP40, MP50…Philips Medizin Systeme Boeblingen GmbH · 2005
  18. 9 generations backK051106 The Philips MP20, MP30, MP40, MP50, MP60, MP70, MP80 and MP90…Philips Medizin Systeme Boeblingen GmbH · 2005
  19. 8 generations backK052801 Intellivue Patient Monitors with Release C.02, Models MP20, MP30…Philips Medizin Systeme Boeblingen GmbH · 2005
  20. 7 generations backK053522 Philips MP40, MP50, MP60, MP70, MP80 and MP90 Intellivue Patient…Philips Medizin Systeme Boeblingen GmbH · 2006
  21. 6 generations backK062271 M3290A Intellivue Information Center Software, Release J.00 (for…Philips Medical Systems · 2006 · Recalled
  22. 5 generations backK081983 M3290A Intellivue Information Center Software, Release 1.00Philips Medical Systems · 2008 · Recalled
  23. 4 generations backK102495 M3290B Intellivue Information Center Software, Release a.0Philips Medical Systems · 2010 · Recalled
  24. 3 generations backK143057 M3290B Philips IntelliVue Information Center iXPhilips Medical Systems · 2014 · Recalled
  25. 2 generations backK153702 M3290B Philips IntelliVue Information Center iXPhilips Medical Systems · 2016 · Recalled
  26. 1 generation backK163584 M3290B Philips IntelliVue Information Center iXPhilips Medical Systems · 2017
  27. This deviceK173203 Athena GTX Device Management Suite (ADMS) SoftwareAthena Gtx · 2018
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−26K941811HP M1175A, M1176A, Component Monitoring SystemHewlett-Packard Co.1994—
−25K960934HP M1205A Omnicare Component Monitor System Model 24Hewlett-Packard Co.1996—
−24K981376Hewlett-Packard M1205A Viridia 24 CTHewlett-Packard Co.1999—
−23K990125HP Viridia Component Monitoring System, Model Rev. KHewlett-Packard GmbH1999—
−22K990972HP Viridia Component Monitoring System, HP Viridia CMS 24/26, HP Viridia…Hewlett-Packard GmbH1999—
−21K013199Philips Component Compact Monitor,Model M1275B, Philips Compenent Rack, Model…Philips Medical Systems, Inc.2001—
−20K020531Philips Multi-Parameter Module, Model M3001A; Philips Component Compact…Philips Medical Systems2002—
−19K021778Philips Component Compact Monitor, Release a.04, Model #M1275BPhilips Medical Systems2002—
−18K023871M3046A (M2/M3/M4) Compact Portable Patient Monitor and MP60 & MP70 Intellivue…Philips Medical Systems2002—
−17K030038Philips MP60, MP70 and MP90 Intellivue Patient Monitors with Portal Technology…Philips Medical Systems, Inc.2003—
−16K031481The Philips Intellivue MP60, MP70, and MP90 Patient Monitors, Release a.20Philips Medizin Systeme Boblingen GmbH2003—
−15K032858The Philips Intellivue MP40, MP50, MP60, MP70,and MP90 Patient Monitors…Philips Medizin Systeme Boblingen GmbH2003—
−14K040304Philips Intellivue Patient Monitor, Models MP40 & MP50Philips Medizin Systeme Boeblingen GmbH2004—
−13K041235Philips MP20, MP30, MP40, MP50. MP60, MP70 and MP90 Intellivue Patient MonitorsPhilips Medizin Systeme Boeblingen GmbH2004—
−12K042845The Philips MP20, MP30, MP40, MP50, MP60, MP70, and MP90 Intellivue Patient…Philips Medizin Systeme Boblingen GmbH2004—
−11K050141The Philips MP20, MP30, MP40, MP50, MP60, MP70 and MP90 Intellivue Patient…Philips Medizin Systeme Boeblingen GmbH2005—
−10K050762Philips Intellivue Patient Monitor, Models MP20, MP30, MP40, MP50, MP60, MP70…Philips Medizin Systeme Boeblingen GmbH2005—
−9K051106The Philips MP20, MP30, MP40, MP50, MP60, MP70, MP80 and MP90 Intellivue…Philips Medizin Systeme Boeblingen GmbH2005—
−8K052801Intellivue Patient Monitors with Release C.02, Models MP20, MP30, MP40, MP50…Philips Medizin Systeme Boeblingen GmbH2005—
−7K053522Philips MP40, MP50, MP60, MP70, MP80 and MP90 Intellivue Patient Monitors…Philips Medizin Systeme Boeblingen GmbH2006—
−6K062271M3290A Intellivue Information Center Software, Release J.00 (for M3140, M3145…Philips Medical Systems20063
−5K081983M3290A Intellivue Information Center Software, Release 1.00Philips Medical Systems20083
−4K102495M3290B Intellivue Information Center Software, Release a.0Philips Medical Systems20107
−3K143057M3290B Philips IntelliVue Information Center iXPhilips Medical Systems20141
−2K153702M3290B Philips IntelliVue Information Center iXPhilips Medical Systems201612
−1K163584M3290B Philips IntelliVue Information Center iXPhilips Medical Systems2017—
0 (this device)K173203Athena GTX Device Management Suite (ADMS) SoftwareAthena Gtx2018—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198710
198920
199060
199170
199260
199360
199430
199560
199680
199770
1998130
1999100
2000200
200160
2002140
200370
2004110
200530
200710
201010
201310
FIG. 1 — Lineage of K173203, 1994–2018Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in MSX? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new MSX device

  1. #1 K242750 Central Stationscore 21.5 · 31 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (2)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K163584M3290B Philips IntelliVue Information Center iX
Summary page 4
…, MLD Basis for Submission: New Device III. PREDICATE DEVICE [807.92(a)(3)]: Legally Marketed (Primary Predicate) Device: M3290B Patient Information Center iX (PIC iX) (K163584) (Second Predicate) Device: WVSM Management Suite (K130957) IV. DEVICE DESCRIPTION [807.92(a)(4)]: Device Identification The At…
Philips Medical Systems2017—
*K130957WVSM (Wirless Vital Signs Monitor)
Summary page 4
…E [807.92(a)(3)]: Legally Marketed (Primary Predicate) Device: M3290B Patient Information Center iX (PIC iX) (K163584) (Second Predicate) Device: WVSM Management Suite (K130957) IV. DEVICE DESCRIPTION [807.92(a)(4)]: Device Identification The Athena GTX Device Management Suite (ADMS) is a software only…
Athena Gtx2013—

Also cleared against K163584: 1 other device →

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 24 years and passes through 7 companies; a new generation was cleared every 5 months on median.
  • 26 of the 165 ancestors have a recall of any class.
  • 1 other device also cites its predicate K163584.

How does its category compare?

All MSX devices

MSX System, Network And Communication, Physiological Monitors: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.

FDA decisions per year · MSX

4in 2025

2007: 42008: 12009: 12010: 32011: 72012: 42013: 22014: 32015: 52016: 32017: 22018: 42019: 42020: 52021: 32022: 52023: 32024: 42025: 42026 (partial year): 5
2007high 7 (2011) · low 1 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MSX

295in 2025

2007: 58 days median2010: 43 days median2011: 72 days median2012: 145 days median2014: 165 days median2015: 138 days median2016: 174 days median2018: 111 days median2019: 92 days median2020: 193 days median2021: 227 days median2022: 177 days median2023: 244 days median2024: 212 days median2025: 295 days median2026 (partial year): 145 days median
2007high 295 (2025) · low 43 (2010)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · MSX

1in 2025

2007: 12008: 12009: 22010: 12011: 12012: 22015: 22017: 22018: 12022: 12025: 12026 (partial year): 2
2007high 2 (2009) · low 0 (2013)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · MSX

19in 2025

2007: 52008: 62009: 72010: 142011: 32012: 42013: 172014: 322015: 312016: 112017: 162018: 152019: 152020: 252021: 172022: 182023: 102024: 322025: 19
2007high 32 (2014) · low 3 (2011)2025

MAUDE reports naming product code MSX, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
200745815
20081—16
20091—27
2010343114
201177213
2012414524
20132—017
20143165032
20155138231
20163174011
20172—216
20184111115
2019492015
20205193025
20213227017
20225177118
20233244010
20244212032
20254295119
202651452—

What is it indicated for?

The intended use of the ADMS software application is to: Receive, aggregate, process, distribute and display physiologic waves, parameters, alarms and events at locations other than at the patient, for multiple patients. Display visual alarm conditions as generated by a connected monitor. Display of patient information can be real-time or historical record review. Provide review and trend application data, designed to contribute to the screening of…

Read the full statement (191 words)

The intended use of the ADMS software application is to:

Receive, aggregate, process, distribute and display physiologic waves, parameters, alarms and events at locations other than at the patient, for multiple patients.

Display visual alarm conditions as generated by a connected monitor.

Display of patient information can be real-time or historical record review.

Provide review and trend application data, designed to contribute to the screening of patient condition.

All information or visual indications provided are intended to support the judgement of a medical professional and are not intended to be the sole source of information for decision making.

Provide connection to other systems not associated with active patient monitoring, such as information systems. The software performs the action to transfer, store, convert from one format to another according to preset specifications, or to display medical device data.

ADMS is intended for use in professional healthcare facilities, emergency medical applications, during transport, and other healthcare environments by trained healthcare professionals. ADMS Software is not intended for home use.

Indicated for use for specific patient populations (adult, pediatric, infant/neonate) depends on the indicated labeling of medical device(s) connected to ADMS providing the data.

Indications for use as stated in the FDA summary.

Also cleared against K163584

1 other device cites the same predicate.

  • K183387M3290B Patient Information Center iXPhilips Medical Systems · 2019

More from Athena Gtx

7 FDA decisions under this applicant name. See the company

  • K191989WVSM (Wireless Vital Signs Monitor) RWC + miniCapAthena Gtx · 2020
  • K160582WiCapAthena Gtx · 2016
  • K153459TacvacAthena Gtx · 2016
  • K130957WVSM (Wirless Vital Signs Monitor)Athena Gtx · 2013
  • K113165Mini-MedicAthena Gtx · 2012

Recent decisions in MSX

The MSX category page

  • K260075eClinicsCeiba Healthcare US, Inc. · 2026
  • K261287Digistat CareAscom Ums Srl Unipersonale · 2026
  • K260211Dashboard (P007000)Hill-Rom, Inc. · 2026
  • K261367Corsano CardioWatch 287-2 SystemCorsano Health B.V. · 2026
  • K253654IntelliVue Measurement Rack 6000 (867317)Philips Medizin Systeme Böblingen GmbH · 2026

https://510kreport.com/device/K173203 · printed Nov 4, 2026

Cite this page

510(k) Report. “K173203: Athena GTX Device Management Suite (ADMS) Software.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K173203

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026