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.

Kentron Health Care, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Kentron Health Care, Inc.

6 devices

1-6 of 6