# Philips Respironics

- Location (FDA's records): Murrysville, PA
- FDA decisions: 2 (2011–2024): 2 510(k) clearances
- Names in FDA's records: Philips Respironics (1); Philips Respironics, Inc. (1)
- Product codes: BZD (1), MNS (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (1 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Respironics, Inc.: 2 (https://510kreport.com/company/respironics)

## Recent decisions
- K233555: AF531 Oro-Nasal EE Leak 1 Face Mask; AF531 Oro-Nasal EE Leak 2 Face Mask (Jul 31, 2024)
- K111378: Oximetry Interface Kit (Oct 4, 2011)

Source page: https://510kreport.com/company/philips-respironics