510(k) · Cleared

Cleared

Apk SPO2 Pulse Oximeter Sensor

K082846510(k) TraditionalCleared Apr 3, 2009186-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

Cleared on Apr 3, 2009 as substantially equivalent to K002223 (Epic Medical Equipment Services, Inc., 2000) after a 186-day review. Its family tree reaches back 1 generation to 2000.

Decided: Apr 3, 2009
Review: 186 days
Class: Class II
Product code: DQA
Recalls: None
Predicates: 1

Its longest line of descent runs back 1 generation to K002223 (2000). No later device cites it as a predicate yet.

By dateBy generation

Root · 1 generation backK002223 Epic SPO2 Finger Sensor, Model E412-20Epic Medical Equipment Services, Inc. · 2000
This deviceK082846 Apk SPO2 Pulse Oximeter SensorAPK Technology Co., Ltd. · 2009

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−1	K002223	Epic SPO2 Finger Sensor, Model E412-20	Epic Medical Equipment Services, Inc.	2000	—
0 (this device)	K082846	Apk SPO2 Pulse Oximeter Sensor	APK Technology Co., Ltd.	2009	—

FIG. 1 — Lineage of K082846, 2000–2009Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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 K221282 Empatica Health Monitoring Platformscore 20.1 · 38 generations · no Class I recall
#2 Held for the reportin the report
#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.

Type	Number	Device	Applicant	Decided	Recalls
*	K002223	Epic SPO2 Finger Sensor, Model E412-20 Summary page 2 …II1510(k) Summary Report No.: TE20080917 Phone: +86-21-64264467 Fax:760-466-5084 Email: Diana.hongzamid-link.net 3. Predicate Device Epic SpO2 Sensor-Model#E412-20(K002223) Manufactured by: Epic Medical Equipment Services,lnc. 1800 E. 10th Street, Suite 300 Plano, TX 75074 4. Device…	Epic Medical Equipment Services, Inc.	2000	—

Also cleared against K002223: 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?

Its one ancestor has no recall.
1 other device also cites its predicate K002223.

How does its category compare?

All DQA devices

DQA Oximeter: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, this device’s year, is highlighted.

FDA decisions per year · DQA

15in 2025

2007high 35 (2009) · low 9 (2017)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DQA

182in 2025

2007high 317 (2023) · low 97 (2008)2026

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

Recalls per year · DQA

3in 2024

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

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

Year	Decisions	Median 510(k) review, days	Recalls (Class I)	MAUDE reports
2007	20	122	6	325
2008	22	97	5	312
2009	35	117	29	281
2010	29	127	4	185
2011	15	195	1	164
2012	14	120	0	322
2013	15	182	0	468
2014	11	175	2	1,124
2015	13	158	1	2,082
2016	14	246	0	1,775
2017	9	200	0	1,190
2018	18	260	32	694
2019	19	158	0	548
2020	15	126	0	426
2021	10	174	0	553
2022	20	265	0	478
2023	13	317	0	392
2024	14	285	3	545
2025	15	182	0	399
2026	8	187	0	—

What is it indicated for?

The APK SpO2 Pulse Oximeter sensor (Reusable) is intended for spot checking or continuous monitoring of functional arterial oxygen saturation and pulse rate in non-invasive with oximeter equipment, which are intended for adult or pediatric patients (more than 5kg) in hospitals, hospital-type facilities, and home environments.

The APK SpO2 Pulse Oximeter sensor (Disposable) is intended for single use when continuous noninvasive arterial oxygen saturation and pulse rate monitoring are adults or pediatric patients (more than 5kg) in hospitals, hospital-type facilities, and home environments.

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K082846 · printed Nov 6, 2026

Cite this page

510(k) Report. “K082846: Apk SPO2 Pulse Oximeter Sensor.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K082846

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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