510(k) · Cleared
ClearedResuscitation Timer, Model L770-CPR
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Allied Healthcare Products, Inc. · BTM Ventilator, Emergency, Manual (Resuscitator)
Cleared on Oct 18, 2006 after an 89-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 4 later devices descend from it.
- Decided
- Oct 18, 2006
- Review
- 89 days
- Class
- Class II
- Product code
- BTM
- Recalls
- None
- Predicates
- 0
4 later devices descend from it, 2 citing it directly.
- This deviceK062080 Resuscitation Timer, Model L770-CPRAllied Healthcare Products, Inc. · 2006
- Descendant · cites it directly · 2 of its ownK141774 Zoll X SeriesZOLL Medical Corporation · 2014
- Descendant · 2 generations on · 1 of its ownK202375 ZOLL Propaq MZOLL Medical Corporation · 2021
- Descendant · 3 generations on · 0 of its ownK233354 WVSM Pro (Series) (500-0030-XX)Athena Gtx, Inc. · 2024
- Descendant · cites it directly · 0 of its ownK221841 EOlife®Archeon · 2023
Most influential descendants
Showing 4 of 4 · See all- K141774Zoll X SeriesZOLL Medical Corporation · 2014 · cites it directly2descendants
- K202375ZOLL Propaq MZOLL Medical Corporation · 2021 · 2 generations on1descendant
- K233354WVSM Pro (Series) (500-0030-XX)Athena Gtx, Inc. · 2024 · 3 generations on0descendants
- K221841EOlife®Archeon · 2023 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K062080 | Resuscitation Timer, Model L770-CPR | Allied Healthcare Products, Inc. | 2006 | — |
| +1 | K141774 | Zoll X Series | ZOLL Medical Corporation | 2014 | — |
| +2 | K202375 | ZOLL Propaq M | ZOLL Medical Corporation | 2021 | — |
| +3 | K233354 | WVSM Pro (Series) (500-0030-XX) | Athena Gtx, Inc. | 2024 | — |
| +1 | K221841 | EOlife® | Archeon | 2023 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2014 | 1 | 0 |
| 2021 | 1 | 0 |
| 2023 | 1 | 0 |
| 2024 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA 510(k) statement (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?
FDA’s file for it is a 510(k) statement, which names no predicate.
What descends from it? (4)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
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?
- Of its descendants, K141774 (ZOLL Medical Corporation, 2014) has gone furthest, with 2 descendants of its own.
How does its category compare?
All BTM devicesBTM Ventilator, Emergency, Manual (Resuscitator): FDA decisions, review times, recalls and adverse event reports over 20 years.
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?
The L770-CPR Resuscitation Timer gives an audible and visual guide to the proper inspiratory time and (BPM) breaths per minute during emergency manual ventilation. It displays the actual inspiratory time, (BPM) breaths per minute, and peak airway pressure.
Indications for use as stated in the FDA 510(k) statement.
https://510kreport.com/device/K062080 · printed Nov 4, 2026
Cite this page
510(k) Report. “K062080: Resuscitation Timer, Model L770-CPR.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K062080
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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