Medical Device Manufacturer · US , Louisville , KY

Dermacare - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1988

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Dermacare General & Plastic Surgery ✕

2 devices

1-2 of 2

Cleared Aug 11, 1989

DERMACARE TIE HOLDER

General & Plastic Surgery · 67d

Cleared Nov 25, 1988

DISPOSABLE BIPOLAR CORD AND BIPOLAR FORCEP

General & Plastic Surgery · 18d