Medical Device Manufacturer · US , Lenexa , KS

Puritan-Bennett - FDA 510(k) Cleared Devices

4 submissions · 3 cleared · Since 1994

Total

Cleared

Denied

Puritan-Bennett has 3 FDA 510(k) cleared medical devices. Based in Lenexa, US.

Historical record: 3 cleared submissions from 1994 to 2002. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Puritan-Bennett

4 devices

1-4 of 4