# K221841: EOlife®

- Pathway: 510(k) (Traditional)
- Applicant: Archeon
- Decided: Mar 18, 2023 after 267 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
Longest line of descent: 1 generation back to K062080 (2006). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062080: Resuscitation Timer, Model L770-CPR, Allied Healthcare Products, Inc. (2006) Summary page 4.

## Indications for use
EOlife is intended for use with emergency manual resuscitation devices to measure ventilatory flows and display visual guide on the insufflated volume, tidal volume, and ventilation frequency to ensure adequate ventilation of adult cardiopulmonary arrest patient during cardiopulmonary resuscitation (CPR) performed by healthcare professionals.

Source page: https://510kreport.com/device/K221841
Methodology: https://510kreport.com/methodology