510(k) Report

510(k) · Cleared

Cleared

All-in-One Health Monitor, PC-303

K170047510(k) TraditionalCleared Sep 9, 2017247-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

Shenzhen Creative Industry Co., Ltd. · MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

Cleared on Sep 9, 2017 as substantially equivalent to K123711 (Shenzhen Creative Industry Co., Ltd., 2013) after a 247-day review. Its family tree reaches back 12 generations to 1994. 1 of the 125 devices in its family, counting itself, has a Class I recall. 6 later devices descend from it.

Decided
Sep 9, 2017
Review
247 days
Class
Class II
Product code
MWI
Recalls
None
Predicates
1

Its longest line of descent runs back 12 generations to K941811 (1994). 118 ancestors in all, the oldest K842616 (1984). 6 later devices descend from it, 3 citing it directly. 1 of the 125 devices in this family, counting this one, has a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 2010: 1 other ancestor2009: 1 other ancestor2006: 1 other ancestor2005: 3 other ancestors2004: 4 other ancestors2002: 5 other ancestors2000: 12 other ancestors2003: 1 other ancestor2001: 2 other ancestors1999: 11 other ancestors1996: 7 other ancestors1995: 9 other ancestors1993: 5 other ancestors1992: 6 other ancestors1990: 5 other ancestors1998: 11 other ancestors1997: 9 other ancestors, 1 with a Class I recall11994: 6 other ancestors1991: 4 other ancestors1989: 1 other ancestor1987: 1 other ancestor1984: 1 other ancestor2021: 1 descendant cleared2024: 2 descendants cleared2026: 1 descendant cleared2022: 1 descendant cleared2023: 1 descendant clearedReference device: K063641 · PC-60, Non-Invasivepulse Oximeter · Shenzhen Creative Industry Co., Ltd. · 2007Reference device: K111463 · Valeo VT-601 Series IR Thermometer · Valeo Corp. · 2012Reference device: K113077 · Bioland G-423 Glood Glucose Monitoring System · Taidoc Technology Corporation · 2012Reference device: K073152 · PC-180 / Prince 180 Easy Ecg Monitor · Shenzhen Creative Industry Co., Ltd. · 2008Reference device: K982140 · Clinical Electronic Thermometer · Valeo Corp. · 1998K941811 · 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) ×5: 5 generations cleared close together, K013199 (2001), K020531 (2002), K021778 (2002), K023871 (2002), K030038 (2003) K053234 · PM-9000 Express Patient Monitor · Shenzhen Mindray Bio-Medical Electronics Co., Ltd. · 2006 · recalledK123711 · Patient Monitor · Shenzhen Creative Industry Co., Ltd. · 201319801990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor3 generations back: 3 other ancestors4 generations back: 9 other ancestors5 generations back: 20 other ancestors6 generations back: 44 other ancestors, 1 with a Class I recall17 generations back: 23 other ancestors8 generations back: 6 other ancestors 1 generation forward: 3 descendants2 generations forward: 3 descendants K123711 · Patient Monitor · Shenzhen Creative Industry Co., Ltd. · 2013K053234 · PM-9000 Express Patient Monitor · Shenzhen Mindray Bio-Medical Electronics Co., Ltd. · 2006 · recalledK030038 · 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. · 1994−10−50
  1. Root · 12 generations backK941811 HP M1175A, M1176A, Component Monitoring SystemHewlett-Packard Co. · 1994
  2. 8 generations between
  3. 3 generations backK030038 Philips MP60, MP70 and MP90 Intellivue Patient Monitors with Portal…Philips Medical Systems, Inc. · 2003
  4. 2 generations backK053234 PM-9000 Express Patient MonitorShenzhen Mindray Bio-Medical Electronics Co., Ltd. · 2006 · Recalled
  5. 1 generation backK123711 Patient MonitorShenzhen Creative Industry Co., Ltd. · 2013
  6. This deviceK170047 All-in-One Health Monitor, PC-303Shenzhen Creative Industry Co., Ltd. · 2017
  7. Descendant · cites it directly · 4 of its ownK210086 Vitals360 Multi-Vitals Mobile MonitorVocare, Inc. · 2021
  8. Descendant · 2 generations on · 1 of its ownK212975 MedWandMedwand Solutions, Inc. · 2022
  9. Descendant · cites it directly · 0 of its ownK253436 c-med0 alphaCosinuss GmbH · 2026
  10. Descendant · 2 generations on · 0 of its ownK231116 Multi-parameter detectorZhongshan Jinli Electronic Weighing Equipment Co., Ltd. · 2024
  11. Descendant · cites it directly · 0 of its ownK231625 VitalDetectWellvii, Inc. · 2024
Show all 12 generations
  1. Root · 12 generations backK941811 HP M1175A, M1176A, Component Monitoring SystemHewlett-Packard Co. · 1994
  2. 11 generations backK960934 HP M1205A Omnicare Component Monitor System Model 24Hewlett-Packard Co. · 1996
  3. 10 generations backK981376 Hewlett-Packard M1205A Viridia 24 CTHewlett-Packard Co. · 1999
  4. 9 generations backK990125 HP Viridia Component Monitoring System, Model Rev. KHewlett-Packard GmbH · 1999
  5. 8 generations backK990972 HP Viridia Component Monitoring System, HP Viridia CMS 24/26, HP…Hewlett-Packard GmbH · 1999
  6. 7 generations backK013199 Philips Component Compact Monitor,Model M1275B, Philips Compenent…Philips Medical Systems, Inc. · 2001
  7. 6 generations backK020531 Philips Multi-Parameter Module, Model M3001A; Philips Component…Philips Medical Systems · 2002
  8. 5 generations backK021778 Philips Component Compact Monitor, Release a.04, Model #M1275BPhilips Medical Systems · 2002
  9. 4 generations backK023871 M3046A (M2/M3/M4) Compact Portable Patient Monitor and MP60 & MP70…Philips Medical Systems · 2002
  10. 3 generations backK030038 Philips MP60, MP70 and MP90 Intellivue Patient Monitors with Portal…Philips Medical Systems, Inc. · 2003
  11. 2 generations backK053234 PM-9000 Express Patient MonitorShenzhen Mindray Bio-Medical Electronics Co., Ltd. · 2006 · Recalled
  12. 1 generation backK123711 Patient MonitorShenzhen Creative Industry Co., Ltd. · 2013
  13. This deviceK170047 All-in-One Health Monitor, PC-303Shenzhen Creative Industry Co., Ltd. · 2017

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

2021: 12022: 12023: 12024: 22026: 1
2021high 2 (2024) · low 0 (2025)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 6 · See all
  • K210086Vitals360 Multi-Vitals Mobile MonitorVocare, Inc. · 2021 · cites it directly4descendants
  • K212975MedWandMedwand Solutions, Inc. · 2022 · 2 generations on1descendant
  • K253436c-med0 alphaCosinuss GmbH · 2026 · cites it directly0descendants
  • K231116Multi-parameter detectorZhongshan Jinli Electronic Weighing Equipment Co., Ltd. · 2024 · 2 generations on0descendants
  • K231625VitalDetectWellvii, Inc. · 2024 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−12K941811HP M1175A, M1176A, Component Monitoring SystemHewlett-Packard Co.1994—
−11K960934HP M1205A Omnicare Component Monitor System Model 24Hewlett-Packard Co.1996—
−10K981376Hewlett-Packard M1205A Viridia 24 CTHewlett-Packard Co.1999—
−9K990125HP Viridia Component Monitoring System, Model Rev. KHewlett-Packard GmbH1999—
−8K990972HP Viridia Component Monitoring System, HP Viridia CMS 24/26, HP Viridia…Hewlett-Packard GmbH1999—
−7K013199Philips Component Compact Monitor,Model M1275B, Philips Compenent Rack, Model…Philips Medical Systems, Inc.2001—
−6K020531Philips Multi-Parameter Module, Model M3001A; Philips Component Compact…Philips Medical Systems2002—
−5K021778Philips Component Compact Monitor, Release a.04, Model #M1275BPhilips Medical Systems2002—
−4K023871M3046A (M2/M3/M4) Compact Portable Patient Monitor and MP60 & MP70 Intellivue…Philips Medical Systems2002—
−3K030038Philips MP60, MP70 and MP90 Intellivue Patient Monitors with Portal Technology…Philips Medical Systems, Inc.2003—
−2K053234PM-9000 Express Patient MonitorShenzhen Mindray Bio-Medical Electronics Co., Ltd.20061
−1K123711Patient MonitorShenzhen Creative Industry Co., Ltd.2013—
0 (this device)K170047All-in-One Health Monitor, PC-303Shenzhen Creative Industry Co., Ltd.2017—
+1K210086Vitals360 Multi-Vitals Mobile MonitorVocare, Inc.2021—
+2K212975MedWandMedwand Solutions, Inc.2022—
+1K253436c-med0 alphaCosinuss GmbH2026—
+2K231116Multi-parameter detectorZhongshan Jinli Electronic Weighing Equipment Co., Ltd.2024—
+1K231625VitalDetectWellvii, Inc.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198410
198710
198910
199050
199140
199260
199350
199460
199590
199670
199791
1998110
1999110
2000120
200120
200250
200310
200440
200530
200610
200910
201010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202110
202210
202310
202420
202610
FIG. 1 — Lineage of K170047, 1994–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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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.

1 device in this family has a Class I recall. 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 MWI device

  1. #1 K230457 Empatica Health Monitoring Platform…score 28.0 · 39 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? (1)

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
*K123711Patient Monitor
Summary page 5
…nufacturer PredicateDevice 510(k) SubmittedDevice Number Shenzhen UP-7000 Patient K123711 All-in-One Health Creative Monitor Monitor, PC-303 Industry Co., Ltd…
Shenzhen Creative Industry Co., Ltd.2013—
†K063641PC-60, Non-Invasivepulse OximeterShenzhen Creative Industry Co., Ltd.2007—
†K111463Valeo VT-601 Series IR ThermometerValeo Corp.2012—
†K113077Bioland G-423 Glood Glucose Monitoring SystemTaidoc Technology Corporation2012—
†K073152PC-180 / Prince 180 Easy Ecg MonitorShenzhen Creative Industry Co., Ltd.2008—
†K982140Clinical Electronic ThermometerValeo Corp.1998—

Also cleared against K123711: 3 other devices →

What descends from it? (6)

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K210086Vitals360 Multi-Vitals Mobile MonitorVocare, Inc.20214
K253436c-med0 alphaCosinuss GmbH20260
K231625VitalDetectWellvii, Inc.20240

Has anything in its family been recalled? (1 Class I)

No FDA recall names this device.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

  • K970209Capnocheck PlusBci Intl., Inc. · 1997 · 6 generations back · ◆ in the 1997 ancestors bar of FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 23 years and passes through 6 companies; a new generation was cleared every 2.1 years on median.
  • 18 of the 118 ancestors have a recall of any class; 1 has a Class I recall.
  • Of its descendants, K210086 (Vocare, Inc., 2021) has gone furthest, with 4 descendants of its own.
  • 3 other devices also cite its predicate K123711.

How does its category compare?

All MWI devices

MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms): FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.

FDA decisions per year · MWI

4in 2025

2007: 92008: 92009: 62010: 172011: 112012: 132013: 202014: 162015: 192016: 122017: 132018: 112019: 142020: 82021: 92022: 52023: 82024: 102025: 42026 (partial year): 6
2007high 20 (2013) · low 4 (2025)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MWI

247in 2025

2007: 42 days median2008: 49 days median2009: 112 days median2010: 58 days median2011: 78 days median2012: 104 days median2013: 85 days median2014: 148 days median2015: 127 days median2016: 165 days median2017: 205 days median2018: 217 days median2019: 255 days median2020: 138 days median2021: 161 days median2022: 231 days median2023: 250 days median2024: 202 days median2025: 247 days median2026 (partial year): 239 days median
2007high 255 (2019) · low 42 (2007)2026

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

Recalls per year · MWI

9so far in 2026, the most since 2007

2007: 12008: 12009: 22010: 22011: 32012: 52013: 32014: 62015: 12017: 22019: 42022: 22024: 52026 (partial year): 9
2007high 9 (2026) · low 0 (2016)2026

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

Adverse event reports per year · MWI

182in 2025

2007: 32008: 32009: 202010: 172011: 162012: 312013: 422014: 302015: 312016: 512017: 852018: 1582019: 1692020: 1102021: 1882022: 1682023: 1792024: 1202025: 182
2007high 188 (2021) · low 3 (2007)2025

MAUDE reports naming product code MWI, 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
200794213
200894913
20096112220
20101758217
20111178316
201213104531
20132085342
201416148630
201519127131
201612165051
201713205285
2018112170158
2019142554169
202081380110
202191610188
202252312168
202382500179
2024102025120
202542470182
202662399—

What is it indicated for?

The All-in-One Health Monitor PC-303 is a device designed for spot-checking measuring of the patient’s physiological parameters, such as Non-Invasive Blood Pressure (NIBP), Oxygen saturation (SpO2), Pulse Rate (PR) and Body Temperature (TEMP);

Additionally, the device is available to communicate with the compatible Blood Glucose Monitoring System and ECG monitor to make the measurement.

This device is applicable for Adult and Pediatric (age≥3 years old) use in clinical institutions and has no conditions or factors of contraindication.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K170047: All-in-One Health Monitor, PC-303.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K170047

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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