Precision Dermatology Incorporated is one of 5383 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Precision Dermatology Incorporated - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Precision Dermatology Incorporated has 3 FDA 510(k) cleared medical devices. Based in Cumberland, US.
Historical record: 3 cleared submissions from 2011 to 2012. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Precision Dermatology Incorporated Filter by specialty or product code using the sidebar.
Precision Dermatology Incorporated — FDA 510(k) Products and Clearance History
3 devices
Cleared
Nov 30, 2012
HYLATOPICPLUS LOTION
General & Plastic Surgery
185d
Cleared
Dec 13, 2011
PRECISION SKIN EMULSION
General & Plastic Surgery
232d
Cleared
Apr 01, 2011
HYLATOPICPLUS CREAM
General & Plastic Surgery
16d