510(k) Report

510(k) · Cleared

Cleared

Reusable & Disposable SpO2 Sensors

K173368510(k) TraditionalCleared Aug 31, 2018309-day reviewClass II21 CFR 870.2700

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

Shenzhen Coreray Technology, Ltd. · DQA Oximeter

Cleared on Aug 31, 2018 as substantially equivalent to K153184 (Shenzhen Caremed Medical Technology Co., Ltd., 2017) and 1 other predicate after a 309-day review. Its family tree reaches back 18 generations to 1994.

Decided
Aug 31, 2018
Review
309 days
Class
Class II
Product code
DQA
Recalls
None
Predicates
2

Its longest line of descent runs back 18 generations to K941811 (1994). 82 ancestors in all, the oldest K863784 (1986). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2010: 1 other ancestor2009: 1 other ancestor2005: 1 other ancestor2004: 3 other ancestors2000: 13 other ancestors1999: 9 other ancestors2007: 1 other ancestor1998: 6 other ancestors1996: 3 other ancestors1989: 1 other ancestor2003: 2 other ancestors1993: 2 other ancestors1990: 2 other ancestors1997: 4 other ancestors1986: 1 other ancestor1995: 3 other ancestors1994: 2 other ancestors1992: 4 other ancestors2002: 2 other ancestors2001: 2 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, K040259 (2004), K041815 (2004) K051212 · Modification to LNCS Oximetry Sensors · Masimo Corporation · 2005 · recalledK101896 · Masimo LNCS/M-LNCS Oximetry Sensors · Masimo Corporation · 2010K111888 · Masimo Lnop/LNCS/M-LNCS Multisite-L Oximetry Sensors · Masimo Corporation · 2011K153184 · Caremed Reusable & Disposable SPO2 Sensors · Shenzhen Caremed Medical Technology Co., Ltd. · 201719851990199520002005201020152020
Other ancestors, by generation 1 generation back: 1 other ancestor2 generations back: 5 other ancestors3 generations back: 9 other ancestors4 generations back: 8 other ancestors5 generations back: 5 other ancestors6 generations back: 5 other ancestors8 generations back: 1 other ancestor9 generations back: 4 other ancestors10 generations back: 23 other ancestors11 generations back: 3 other ancestors K153184 · Caremed Reusable & Disposable SPO2 Sensors · Shenzhen Caremed Medical Technology Co., Ltd. · 2017K111888 · Masimo Lnop/LNCS/M-LNCS Multisite-L Oximetry Sensors · Masimo Corporation · 2011K101896 · Masimo LNCS/M-LNCS Oximetry Sensors · Masimo Corporation · 2010K051212 · Modification to LNCS Oximetry Sensors · Masimo Corporation · 2005 · recalledK041815 · LNCS Oximetry Sensors · Masimo Corp. · 2004K040259 · Masimo Set Intellivue Pulse Oximeter Module · Masimo Corp. · 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. · 1994−15−10−50
  1. Root · 18 generations backK941811 HP M1175A, M1176A, Component Monitoring SystemHewlett-Packard Co. · 1994
  2. 14 generations between
  3. 3 generations backK101896 Masimo LNCS/M-LNCS Oximetry SensorsMasimo Corporation · 2010
  4. 2 generations backK111888 Masimo Lnop/LNCS/M-LNCS Multisite-L Oximetry SensorsMasimo Corporation · 2011
  5. 1 generation backK153184 Caremed Reusable & Disposable SPO2 SensorsShenzhen Caremed Medical Technology Co., Ltd. · 2017
  6. This deviceK173368 Reusable & Disposable SpO2 SensorsShenzhen Coreray Technology, Ltd. · 2018
Show all 18 generations
  1. Root · 18 generations backK941811 HP M1175A, M1176A, Component Monitoring SystemHewlett-Packard Co. · 1994
  2. 17 generations backK960934 HP M1205A Omnicare Component Monitor System Model 24Hewlett-Packard Co. · 1996
  3. 16 generations backK981376 Hewlett-Packard M1205A Viridia 24 CTHewlett-Packard Co. · 1999
  4. 15 generations backK990125 HP Viridia Component Monitoring System, Model Rev. KHewlett-Packard GmbH · 1999
  5. 14 generations backK990972 HP Viridia Component Monitoring System, HP Viridia CMS 24/26, HP…Hewlett-Packard GmbH · 1999
  6. 13 generations backK013199 Philips Component Compact Monitor,Model M1275B, Philips Compenent…Philips Medical Systems, Inc. · 2001
  7. 12 generations backK020531 Philips Multi-Parameter Module, Model M3001A; Philips Component…Philips Medical Systems · 2002
  8. 11 generations backK021778 Philips Component Compact Monitor, Release a.04, Model #M1275BPhilips Medical Systems · 2002
  9. 10 generations backK023871 M3046A (M2/M3/M4) Compact Portable Patient Monitor and MP60 & MP70…Philips Medical Systems · 2002
  10. 9 generations backK030038 Philips MP60, MP70 and MP90 Intellivue Patient Monitors with Portal…Philips Medical Systems, Inc. · 2003
  11. 8 generations backK031481 The Philips Intellivue MP60, MP70, and MP90 Patient Monitors…Philips Medizin Systeme Boblingen GmbH · 2003
  12. 7 generations backK032858 The Philips Intellivue MP40, MP50, MP60, MP70,and MP90 Patient…Philips Medizin Systeme Boblingen GmbH · 2003
  13. 6 generations backK040259 Masimo Set Intellivue Pulse Oximeter ModuleMasimo Corp. · 2004
  14. 5 generations backK041815 LNCS Oximetry SensorsMasimo Corp. · 2004
  15. 4 generations backK051212 Modification to LNCS Oximetry SensorsMasimo Corporation · 2005 · Recalled
  16. 3 generations backK101896 Masimo LNCS/M-LNCS Oximetry SensorsMasimo Corporation · 2010
  17. 2 generations backK111888 Masimo Lnop/LNCS/M-LNCS Multisite-L Oximetry SensorsMasimo Corporation · 2011
  18. 1 generation backK153184 Caremed Reusable & Disposable SPO2 SensorsShenzhen Caremed Medical Technology Co., Ltd. · 2017
  19. This deviceK173368 Reusable & Disposable SpO2 SensorsShenzhen Coreray Technology, Ltd. · 2018
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−18K941811HP M1175A, M1176A, Component Monitoring SystemHewlett-Packard Co.1994—
−17K960934HP M1205A Omnicare Component Monitor System Model 24Hewlett-Packard Co.1996—
−16K981376Hewlett-Packard M1205A Viridia 24 CTHewlett-Packard Co.1999—
−15K990125HP Viridia Component Monitoring System, Model Rev. KHewlett-Packard GmbH1999—
−14K990972HP Viridia Component Monitoring System, HP Viridia CMS 24/26, HP Viridia…Hewlett-Packard GmbH1999—
−13K013199Philips Component Compact Monitor,Model M1275B, Philips Compenent Rack, Model…Philips Medical Systems, Inc.2001—
−12K020531Philips Multi-Parameter Module, Model M3001A; Philips Component Compact…Philips Medical Systems2002—
−11K021778Philips Component Compact Monitor, Release a.04, Model #M1275BPhilips Medical Systems2002—
−10K023871M3046A (M2/M3/M4) Compact Portable Patient Monitor and MP60 & MP70 Intellivue…Philips Medical Systems2002—
−9K030038Philips MP60, MP70 and MP90 Intellivue Patient Monitors with Portal Technology…Philips Medical Systems, Inc.2003—
−8K031481The Philips Intellivue MP60, MP70, and MP90 Patient Monitors, Release a.20Philips Medizin Systeme Boblingen GmbH2003—
−7K032858The Philips Intellivue MP40, MP50, MP60, MP70,and MP90 Patient Monitors…Philips Medizin Systeme Boblingen GmbH2003—
−6K040259Masimo Set Intellivue Pulse Oximeter ModuleMasimo Corp.2004—
−5K041815LNCS Oximetry SensorsMasimo Corp.2004—
−4K051212Modification to LNCS Oximetry SensorsMasimo Corporation20055
−3K101896Masimo LNCS/M-LNCS Oximetry SensorsMasimo Corporation2010—
−2K111888Masimo Lnop/LNCS/M-LNCS Multisite-L Oximetry SensorsMasimo Corporation2011—
−1K153184Caremed Reusable & Disposable SPO2 SensorsShenzhen Caremed Medical Technology Co., Ltd.2017—
0 (this device)K173368Reusable & Disposable SpO2 SensorsShenzhen Coreray Technology, Ltd.2018—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198610
198710
198910
199020
199240
199320
199420
199530
199630
199740
199860
199990
2000130
200120
200220
200320
200430
200510
200710
200910
201010
FIG. 1 — Lineage of K173368, 1994–2018Source: 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.

Planning a device in DQA? 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 DQA device

  1. #1 K221282 Empatica Health Monitoring Platformscore 20.1 · 38 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
*K153184Caremed Reusable & Disposable SPO2 Sensors
Summary page 5
…e Information Sponsor: Shenzhen Caremed Medical Technology Co., Ltd. Device: Caremed Reusable & Disposable SpO2 Sensors 510(K) Number: K153184 Sponsor: Solaris Medical Technology, Inc. Device: Solaris Reusable & Disposable SPO2 Sensors…
Shenzhen Caremed Medical Technology Co., Ltd.2017—
*K100077Nellcor Compatible Reusable SPO2 Soft-Finger Sensor, Model T100A-090103
Summary page 5
…510(K) Number: K153184 Sponsor: Solaris Medical Technology, Inc. Device: Solaris Reusable & Disposable SPO2 Sensors 510(K) Number: K100077 5.4 Device Description The Reusable SPO 2 Sensor is comprised of a connector and a cable which terminates into sensor housing.…
Solaris Medical Technology, Inc.2010—

Also cleared against K153184: 3 other devices →

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 9 companies; a new generation was cleared every 6 months on median.
  • 6 of the 82 ancestors have a recall of any class.
  • 3 other devices also cite its predicate K153184.

How does its category compare?

All DQA devices

DQA Oximeter: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.

FDA decisions per year · DQA

15in 2025

2007: 202008: 222009: 352010: 292011: 152012: 142013: 152014: 112015: 132016: 142017: 92018: 182019: 192020: 152021: 102022: 202023: 132024: 142025: 152026 (partial year): 8
2007high 35 (2009) · low 9 (2017)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DQA

182in 2025

2007: 122 days median2008: 97 days median2009: 117 days median2010: 127 days median2011: 195 days median2012: 120 days median2013: 182 days median2014: 175 days median2015: 158 days median2016: 246 days median2017: 200 days median2018: 260 days median2019: 158 days median2020: 126 days median2021: 174 days median2022: 265 days median2023: 317 days median2024: 285 days median2025: 182 days median2026 (partial year): 187 days median
2007high 317 (2023) · low 97 (2008)2026

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

Recalls per year · DQA

3in 2024

2007: 62008: 52009: 292010: 42011: 12014: 22015: 12018: 322024: 3
2007high 32 (2018) · low 0 (2012)2026

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

Adverse event reports per year · DQA

399in 2025

2007: 3252008: 3122009: 2812010: 1852011: 1642012: 3222013: 4682014: 1,1242015: 2,0822016: 1,7752017: 1,1902018: 6942019: 5482020: 4262021: 5532022: 4782023: 3922024: 5452025: 399
2007high 2,082 (2015) · low 164 (2011)2025

MAUDE reports naming product code DQA, 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
2007201226325
200822975312
20093511729281
2010291274185
2011151951164
2012141200322
2013151820468
20141117521,124
20151315812,082
20161424601,775
2017920001,190
20181826032694
2019191580548
2020151260426
2021101740553
2022202650478
2023133170392
2024142853545
2025151820399
202681870—

What is it indicated for?

Coreray Reusable SPO2 Sensor is intended to be used in hospital settings where patient care is offered by qualified healthcare personnel. The Reusable SPO2 Sensor is intended for continuous non-invasive monitoring of functional oxygen saturation of arterial hemoglobin (SpO2) and pulse rate(PR) for adult patients weighing greater than 40kg.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K173368: Reusable & Disposable SpO2 Sensors.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K173368

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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