Medical Device Manufacturer · US , Coconut Creek , FL

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

3 submissions · 3 cleared · Since 2005

Total

Cleared

Denied

Respcare, Inc. has 3 FDA 510(k) cleared medical devices. Based in Coconut Creek, US.

Historical record: 3 cleared submissions from 2005 to 2006. Primary specialty: Anesthesiology.

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

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

3 devices

1-3 of 3