Medical Device Manufacturer · US , Palo Alto , CA

Pulmonx - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1998

Total

Cleared

Denied

Pulmonx has 1 FDA 510(k) cleared medical devices. Based in Palo Alto, US.

Historical record: 1 cleared submissions from 1998 to 1998. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Pulmonx Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Pulmonx

1 devices

1-1 of 1