Medical Device Manufacturer · US , Tonawanda , NY

Praxair, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2005

Total

Cleared

Denied

Praxair, Inc. has 2 FDA 510(k) cleared medical devices. Based in Tonawanda, US.

Historical record: 2 cleared submissions from 2005 to 2020. Primary specialty: Anesthesiology.

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

FDA 510(k) cleared devices by Praxair, Inc.

2 devices

1-2 of 2