# K062080: Resuscitation Timer, Model L770-CPR

- Pathway: 510(k) (Traditional)
- Applicant: Allied Healthcare Products, Inc.
- Decided: Oct 18, 2006 after 89 days
- Product code: BTM (Ventilator, Emergency, Manual (Resuscitator))
- Device class: 2
- Regulation: 21 CFR 868.5915
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 2 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K141774: Zoll X Series (2014), 2 descendants of its own
- K202375: ZOLL Propaq M (2021), 1 descendant of its own
- K233354: WVSM Pro (Series) (500-0030-XX) (2024), 0 descendants of its own
- K221841: EOlife® (2023), 0 descendants of its own

## Indications for use
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.

Source page: https://510kreport.com/device/K062080
Methodology: https://510kreport.com/methodology