Medical Device Manufacturer · US , Palo Alto , CA

Pulmonx - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1998

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Pulmonx Anesthesiology ✕

1 devices

1-1 of 1

Cleared Feb 13, 1998

THE VISUALIZED ENDOTRACHEAL TUBE SYSTEM OR VETT SYSTEM

Anesthesiology · 172d