Precision Dermatology Incorporated is one of 5706 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.
FDA 510(k) Regulatory Record - Precision Dermatology Incorporated
3 devices