Medical Device Manufacturer · DE , Boblingen

Philips Medizin Systeme - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2026

Recent clearances: Nasal Alar SpO2 Sensor (989803205381)

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Philips Medizin Systeme Anesthesiology ✕

1 devices

1-1 of 1

Cleared May 01, 2026

Nasal Alar SpO2 Sensor (989803205381)

Anesthesiology · 148d