Philips Respironics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Philips Respironics - FDA 510(k) Cleared Devices
Recent clearances: AF531 Oro-Nasal EE Leak 1 Face Mask
1
Total
1
Cleared
0
Denied
Philips Respironics has 1 FDA 510(k) cleared medical devices. Based in Murrysville, US.
Latest FDA clearance: Jul 2024. Active since 2024. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Philips Respironics Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Philips Respironics
1 devices