510(k) · Cleared
ClearedDisposable Manual Resuscitator
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Xiamen Compower Medical Tech. Co., Ltd. · BTM Ventilator, Emergency, Manual (Resuscitator)
Cleared on Aug 26, 2021 as substantially equivalent to K170663 (Foremount Enterprise Co., Ltd., 2018) after a 205-day review. Its family tree reaches back 3 generations to 1990.
- Decided
- Aug 26, 2021
- Review
- 205 days
- Class
- Class II
- Product code
- BTM
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 3 generations to K902062 (1990). 5 ancestors in all. No later device cites it as a predicate yet.
- Root · 3 generations backK902062 Peep ValveHudson Oxygen Therapy Sales Co. · 1990
- 2 generations backK082092 Dispo-Bag Manual Resuscitator, Disposable Adjustable Peep Valve…Galemed Corp. · 2008
- 1 generation backK170663 Foremount Disposable PVC Resuscitator, Foremount Disposable PEEP…Foremount Enterprise Co., Ltd. · 2018
- This deviceK210288 Disposable Manual ResuscitatorXiamen Compower Medical Tech. Co., Ltd. · 2021
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K902062 | Peep Valve | Hudson Oxygen Therapy Sales Co. | 1990 | — |
| −2 | K082092 | Dispo-Bag Manual Resuscitator, Disposable Adjustable Peep Valve, Disposable… | Galemed Corp. | 2008 | — |
| −1 | K170663 | Foremount Disposable PVC Resuscitator, Foremount Disposable PEEP Valve… | Foremount Enterprise Co., Ltd. | 2018 | — |
| 0 (this device) | K210288 | Disposable Manual Resuscitator | Xiamen Compower Medical Tech. Co., Ltd. | 2021 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1994 | 1 | 0 |
| 2013 | 1 | 0 |
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 BTM? 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 BTM device
- #1 K243861 butterflyBVMscore 9.5 · 2 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K170663 | Foremount Disposable PVC Resuscitator, Foremount Disposable PEEP Valve, Foremount…Summary page 5…page 6- 2 006 510(k) Summary 8 Legally Marketed Predicate Device Foremount Disposable PVC Resuscitator Model A1 K170663 Code BTM 9 Predicate Device Company Foremount Enterprise Co., Ltd. 10 Device Description… | 2018 |
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 31 years and passes through 4 companies; a new generation was cleared every 9.6 years on median.
- None of the 5 ancestors has a recall.
How does its category compare?
All BTM devicesBTM Ventilator, Emergency, Manual (Resuscitator): FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.
FDA decisions per year · BTM
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · BTM
83in 2008
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · BTM
9in 2024
Class I (24 since 2007) Class II/III not classified
Adverse event reports per year · BTM
36in 2025
MAUDE reports naming product code BTM, 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 | 2 | — | 0 | 65 |
| 2008 | 3 | 83 | 0 | 31 |
| 2009 | 0 | — | 23 | 21 |
| 2010 | 2 | — | 3 | 23 |
| 2011 | 2 | — | 0 | 48 |
| 2012 | 1 | — | 13 (13) | 69 |
| 2013 | 0 | — | 3 (1) | 44 |
| 2014 | 0 | — | 0 | 108 |
| 2015 | 1 | — | 0 | 36 |
| 2016 | 1 | — | 0 | 92 |
| 2017 | 0 | — | 0 | 56 |
| 2018 | 2 | — | 0 | 56 |
| 2019 | 0 | — | 0 | 46 |
| 2020 | 0 | — | 0 | 26 |
| 2021 | 1 | — | 0 | 42 |
| 2022 | 1 | — | 0 | 35 |
| 2023 | 1 | — | 9 | 46 |
| 2024 | 0 | — | 9 (9) | 33 |
| 2025 | 2 | — | 0 | 36 |
| 2026 | 1 | — | 1 (1) | — |
What is it indicated for?
Single patient use manual resuscitator for use in hospital, transport, emergency, and post-hospital care to temporary
ventilate a patient for the given body mass ranges of:
Infant: less than or equal to 10 kg
Child: less than or equal to 23 kg
Adult: greater than 23 kg
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K210288 · printed Nov 6, 2026
Cite this page
510(k) Report. “K210288: Disposable Manual Resuscitator.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K210288
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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