Medical Device Manufacturer · US , Hollywood , FL

Kentron Health Care, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1995

Total

Cleared

Denied

Kentron Health Care, Inc. has 6 FDA 510(k) cleared medical devices. Based in Hollywood, US.

Historical record: 6 cleared submissions from 1995 to 2003. Primary specialty: General Hospital.

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

6 devices

1–6 of 6