510(k) Report

510(k) · Cleared

Cleared

Pulse Oximeter

K173123510(k) TraditionalCleared Aug 13, 2018318-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 Imdk Medical Technology Co., Ltd. · DQA Oximeter

Cleared on Aug 13, 2018 as substantially equivalent to K153021 (Amemo, Inc., 2016) after a 318-day review. Its family tree reaches back 5 generations to 2000. 11 later devices descend from it.

Decided
Aug 13, 2018
Review
318 days
Class
Class II
Product code
DQA
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K001085 (2000). 11 later devices descend from it, 4 citing it directly.

  1. Root · 5 generations backK001085 Modification to Onyx, Finger Clip Pulse Oximeter, Model 9500Nonin Medical, Inc. · 2000
  2. 4 generations backK051107 Onyx II Finger Pulse Oximeter, Model 9550Nonin Medical, Inc. · 2005
  3. 3 generations backK070371 Fingertip Pulse Oximeter MD300CBeijing Choice Electronic Technololgy Co., Ltd. · 2007
  4. 2 generations backK093757 MD300C1 Fingertip Pulse OximeterBeijing Choice Electronic Technololgy Co., Ltd. · 2010
  5. 1 generation backK153021 Fingertip Pulse Oximeter A310Amemo, Inc. · 2016
  6. This deviceK173123 Pulse OximeterShenzhen Imdk Medical Technology Co., Ltd. · 2018
  7. Descendant · cites it directly · 7 of its ownK191430 Pulse OximeterShenzhen Yimi Life-Technology Co., Ltd. · 2019
  8. Descendant · 2 generations on · 1 of its ownK212665 Pulse Oximeter (Model Number-SO611), Pulse Oximeter (Model Number-…Huizhou Xiaoou Technology Co., Ltd. · 2022
  9. Descendant · 2 generations on · 1 of its ownK202173 Pulse OximeterShenzhen AOJ Medical Technology Co., Ltd. · 2020
  10. Descendant · cites it directly · 0 of its ownK252655 Pulse Oximeter (PO-A2AO, PO-A2AT, PO-A3AO, PO-H1AO, PO-B1AO…Shenzhen Imdk Medical Technology Co., Ltd. · 2026
  11. Descendant · 3 generations on · 0 of its ownK232520 Fingertip Pulse Oximeter, models Alpine20, Alpine20A, Alpine20H…Shenzhen Smallsignal Technology Co., Ltd. · 2024

Showing 5 of 11 descendants. See all descendants

Descendants cleared per year

2019: 12020: 32022: 22023: 12024: 32026: 1
2019high 3 (2020) · low 0 (2021)2026

Most influential descendants

Showing 5 of 11 · See all
  • K191430Pulse OximeterShenzhen Yimi Life-Technology Co., Ltd. · 2019 · cites it directly7descendants
  • K212665Pulse Oximeter (Model Number-SO611), Pulse Oximeter (Model Number- S0711), Pulse…Huizhou Xiaoou Technology Co., Ltd. · 2022 · 2 generations on1descendant
  • K202173Pulse OximeterShenzhen AOJ Medical Technology Co., Ltd. · 2020 · 2 generations on1descendant
  • K252655Pulse Oximeter (PO-A2AO, PO-A2AT, PO-A3AO, PO-H1AO, PO-B1AO, PO-C5AO, PO-C5AT, PO-C6AO…Shenzhen Imdk Medical Technology Co., Ltd. · 2026 · cites it directly0descendants
  • K232520Fingertip Pulse Oximeter, models Alpine20, Alpine20A, Alpine20H, Alpine20HA, Alpine20B…Shenzhen Smallsignal Technology Co., Ltd. · 2024 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K001085Modification to Onyx, Finger Clip Pulse Oximeter, Model 9500Nonin Medical, Inc.2000—
−4K051107Onyx II Finger Pulse Oximeter, Model 9550Nonin Medical, Inc.2005—
−3K070371Fingertip Pulse Oximeter MD300CBeijing Choice Electronic Technololgy Co., Ltd.2007—
−2K093757MD300C1 Fingertip Pulse OximeterBeijing Choice Electronic Technololgy Co., Ltd.2010—
−1K153021Fingertip Pulse Oximeter A310Amemo, Inc.2016—
0 (this device)K173123Pulse OximeterShenzhen Imdk Medical Technology Co., Ltd.2018—
+1K191430Pulse OximeterShenzhen Yimi Life-Technology Co., Ltd.2019—
+2K212665Pulse Oximeter (Model Number-SO611), Pulse Oximeter (Model Number- S0711)…Huizhou Xiaoou Technology Co., Ltd.2022—
+2K202173Pulse OximeterShenzhen AOJ Medical Technology Co., Ltd.2020—
+1K252655Pulse Oximeter (PO-A2AO, PO-A2AT, PO-A3AO, PO-H1AO, PO-B1AO, PO-C5AO, PO-C5AT…Shenzhen Imdk Medical Technology Co., Ltd.2026—
+3K232520Fingertip Pulse Oximeter, models Alpine20, Alpine20A, Alpine20H, Alpine20HA…Shenzhen Smallsignal Technology Co., Ltd.2024—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201910
202030
202220
202310
202430
202610
FIG. 1 — Lineage of K173123, 2000–2026Source: 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.

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
*K153021Fingertip Pulse Oximeter A310
Summary page 4
…21CFR 870.2700 / Oximeter / DQA Submission type Traditional 510(K) 4. Predicate Device AMEMO Inc. Fingertip Pulse Oximeter A310/ K153021. The subject device has same intended use, same target patient population, and same performance effectiveness as the predicate de…
Amemo, Inc.2016—

Also cleared against K153021: 1 other device →

What descends from it? (11)

See all 11

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

NumberDeviceApplicantDecidedDescendants
K191430Pulse OximeterShenzhen Yimi Life-Technology Co., Ltd.20197
K252655Pulse Oximeter (PO-A2AO, PO-A2AT, PO-A3AO, PO-H1AO, PO-B1AO, PO-C5AO, PO-C5AT, PO-C6AO…Shenzhen Imdk Medical Technology Co., Ltd.20260
K211143Pulse OximeterShenzhen Brav Electronic Technologies Co., Ltd.20230
K221979Pulse Oximeter (Model C101A2, C101B1, C101A3)Shenzhen Imdk Medical Technology Co., Ltd.20220

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 18 years and passes through 4 companies; a new generation was cleared every 2.6 years on median.
  • None of the 5 ancestors has a recall.
  • Of its descendants, K191430 (Shenzhen Yimi Life-Technology Co., Ltd., 2019) has gone furthest, with 7 descendants of its own.
  • 1 other device also cites its predicate K153021.

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?

Fingertip Pulse Oximeter C101H1 is a non-invasive device intended for spot checking of functional oxygen saturation of arterial hemoglobin (SpO2) and pulse rate (PR). This portable device is indicated for use in adult patients in hospitals.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K173123: Pulse Oximeter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K173123

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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