# K880450: Resusci Patient Face Shield

- Pathway: 510(k) (Traditional)
- Applicant: Laerdal Medical Corp.
- Decided: Mar 4, 1988 after 31 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K980066: CPR Filtershield (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K880450
Methodology: https://510kreport.com/methodology