Medical Device Manufacturer · US , N. Ft. Myers , FL

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

3 submissions · 3 cleared · Since 1994

Total

Cleared

Denied

Oxlife, Inc. has 3 FDA 510(k) cleared medical devices. Based in N. Ft. Myers, US.

Historical record: 3 cleared submissions from 1994 to 1997. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Oxlife, Inc.

3 devices

1-3 of 3