510(k) Report

510(k) · Cleared

Cleared

Masimo Rainbow Set Radcheck Pulse CO-Oximeter, Radcheck, Rad 57 Spot Check

K082052510(k) TraditionalCleared Oct 10, 200881-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

Masimo Corporation · DQA Oximeter

Cleared on Oct 10, 2008 as substantially equivalent to K080238 (Masimo Corporation, 2008) after an 81-day review. Its family tree reaches back 7 generations to 2000. 6 later devices descend from it.

Decided
Oct 10, 2008
Review
81 days
Class
Class II
Product code
DQA
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K000126 (2000). 9 ancestors in all, the oldest K853990 (1985). 6 later devices descend from it, 2 citing it directly.

  1. Root · 7 generations backK000126 Masimo Set Radical Pulse Oximeter with Satshare, Masimo…Masimo Corp. · 2000
  2. 6 generations backK031330 Modification to Masimo Set Radical Pulse Oximeter with Satshare and…Masimo Corp. · 2003
  3. 5 generations backK033296 Masimo Set Rad-5 Pulse Oximeter, Model Rad-5; Masimo Set Rad-5V…Masimo Corp. · 2004 · Recalled
  4. 4 generations backK042536 Masimo Set Rad 57 Pulse CO-OximeterMasimo Corporation · 2005 · Recalled
  5. 3 generations backK053477 Masimo Set Rad 57 CM and M Pulse CO-OximetersMasimo Corporation · 2006
  6. 2 generations backK061204 Masimo Set Radical 7 Pulse CO-OximeterMasimo Corporation · 2006
  7. 1 generation backK080238 Masimo Rainbow Set Radical 7 Pulse CO-Oximeter, Masimo Rainbow Set…Masimo Corporation · 2008 · Recalled
  8. This deviceK082052 Masimo Rainbow Set Radcheck Pulse CO-Oximeter, Radcheck, Rad 57 Spot…Masimo Corporation · 2008
  9. Descendant · cites it directly · 5 of its ownK091057 Masimo Rainbow Set Pronto Pulse CO-Oximeter and AccessoriesMasimo Corporation · 2009
  10. Descendant · cites it directly · 1 of its ownK124041 NBM-200MPOrsense, Ltd. · 2013
  11. Descendant · 2 generations on · 1 of its ownK100403 Masimo Rainbow Set Pronto -7 Pulse CO- Oximeter and Accessories…Masimo Corporation · 2010 · Recalled
  12. Descendant · 2 generations on · 0 of its ownK182887 Masimo Rad-67 Pulse CO-Oximeter and AccessoriesMasimo Corporation · 2019
  13. Descendant · 2 generations on · 0 of its ownK142209 Pulse oximeter NBM-200Orsense, Ltd. · 2015

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

2009: 12010: 12011: 12013: 12015: 12019: 1
2009high 1 (2009) · low 0 (2012)2026

Most influential descendants

Showing 5 of 6 · See all
  • K091057Masimo Rainbow Set Pronto Pulse CO-Oximeter and AccessoriesMasimo Corporation · 2009 · cites it directly5descendants
  • K124041NBM-200MPOrsense, Ltd. · 2013 · cites it directly1descendant
  • K100403Masimo Rainbow Set Pronto -7 Pulse CO- Oximeter and Accessories, Model Pronto-7Masimo Corporation · 2010 · 2 generations on1descendant
  • K182887Masimo Rad-67 Pulse CO-Oximeter and AccessoriesMasimo Corporation · 2019 · 2 generations on0descendants
  • K142209Pulse oximeter NBM-200Orsense, Ltd. · 2015 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K000126Masimo Set Radical Pulse Oximeter with Satshare, Masimo…Masimo Corp.2000—
−6K031330Modification to Masimo Set Radical Pulse Oximeter with Satshare and Lnop…Masimo Corp.2003—
−5K033296Masimo Set Rad-5 Pulse Oximeter, Model Rad-5; Masimo Set Rad-5V Pulse…Masimo Corp.20041
−4K042536Masimo Set Rad 57 Pulse CO-OximeterMasimo Corporation20051
−3K053477Masimo Set Rad 57 CM and M Pulse CO-OximetersMasimo Corporation2006—
−2K061204Masimo Set Radical 7 Pulse CO-OximeterMasimo Corporation2006—
−1K080238Masimo Rainbow Set Radical 7 Pulse CO-Oximeter, Masimo Rainbow Set Rad 87…Masimo Corporation20081
0 (this device)K082052Masimo Rainbow Set Radcheck Pulse CO-Oximeter, Radcheck, Rad 57 Spot CheckMasimo Corporation2008—
+1K091057Masimo Rainbow Set Pronto Pulse CO-Oximeter and AccessoriesMasimo Corporation2009—
+1K124041NBM-200MPOrsense, Ltd.2013—
+2K100403Masimo Rainbow Set Pronto -7 Pulse CO- Oximeter and Accessories, Model Pronto-7Masimo Corporation20101
+2K182887Masimo Rad-67 Pulse CO-Oximeter and AccessoriesMasimo Corporation2019—
+2K142209Pulse oximeter NBM-200Orsense, Ltd.2015—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198510
200410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200910
201010
201110
201310
201510
201910
FIG. 1 — Lineage of K082052, 2000–2019Source: 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
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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
*K080238Masimo Rainbow Set Radical 7 Pulse CO-Oximeter, Masimo Rainbow Set Rad 87 Pulse…
Summary page 1
…Substantially Equivalent Devices: Masimo Rainbow SET Rad 57t Pulse CO-Oximeters and Accessories, 510(k) Number K080238 Device Description The Masimo Rainbow SETO RadCheck Pulse CO-Oximeter and Accessories (RadCheck) have modified intended use/…
Masimo Corporation20081

Also cleared against K080238: 10 other devices →

What descends from it? (6)

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

NumberDeviceApplicantDecidedDescendants
K091057Masimo Rainbow Set Pronto Pulse CO-Oximeter and AccessoriesMasimo Corporation20095
K124041NBM-200MPOrsense, Ltd.20131

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 8 years and passes through 2 companies; a new generation was cleared every 11 months on median.
  • 3 of the 9 ancestors have a recall of any class.
  • Of its descendants, K091057 (Masimo Corporation, 2009) has gone furthest, with 5 descendants of its own.
  • 10 other devices also cite its predicate K080238.

How does its category compare?

All DQA devices

DQA Oximeter: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, 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?

The Masimo Rainbow SET RadCheck Pulse CO-Oximeter and Accessories are indicated for noninvasive spot checking of functional saturation of arterial hemoglobin (SpO2), pulse rate, and total hemoglobin (SpHb). The Masimo Rainbow SET RadCheck Pulse CO-Oximeter and Accessories are indicated for use, by trained personnel, with adult and pediatric patients during both no motion and motion conditions, and for patients who are well or poorly perfused in clinical and non-clinical settings.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K082052: Masimo Rainbow Set Radcheck Pulse CO-Oximeter, Radcheck, Rad 57 Spot Check.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K082052

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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