# K932170: Flynnr Genesis II a/C, a/O and Idlh

- Pathway: 510(k) (Traditional)
- Applicant: O-Two Systems Intl., Inc.
- Decided: Oct 25, 1993 after 174 days
- Product code: BTL (Ventilator, Emergency, Powered (Resuscitator))
- Device class: 2
- Regulation: 21 CFR 868.5925
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
13 later devices descend from it; 6 cite it directly.
1 of 14 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K983857: Autovent 1500 (1998), 6 descendants of its own
- K983785: Autovent 1000 (1998), 6 descendants of its own
- K983643: Genesis BLS (1998), 6 descendants of its own
- K991195: Carevent BLS, Carevent BLS+, Carevent Als, Carevent Als+, and Carevent Atv (1999), 5 descendants of its own
- K081330: Carevent Par (Public Access Resuscitator) (2009), 2 descendants of its own

Source page: https://510kreport.com/device/K932170
Methodology: https://510kreport.com/methodology