# Bunnell, Inc.

- Location (FDA's records): Salt Lake City
- FDA decisions: 1 (1988–1988): 1 original PMA approval
- Product codes: LSZ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 4 (1 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- P850064: Model 203 Life Pulse High Frequency Ventilator (Jun 30, 1988)

Source page: https://510kreport.com/company/bunnell