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.

Pulmonx is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Pulmonx

1 devices

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