Medical Device Manufacturer · US , Louisville , KT

Dermacare Products, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1985

Total

Cleared

Denied

Dermacare Products, Inc. has 8 FDA 510(k) cleared medical devices. Based in Louisville, US.

Historical record: 8 cleared submissions from 1985 to 1988. Primary specialty: General & Plastic Surgery.

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

Dermacare Products, 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 - Dermacare Products, Inc.

8 devices

1-8 of 8