Stefanovsky & Assoc. is one of 14456 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stefanovsky & Assoc. - FDA 510(k) Cleared Devices
Recent clearances: LASER EYE GOGGLES
3
Total
3
Cleared
0
Denied
Stefanovsky & Assoc. has 3 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 3 cleared submissions from 1983 to 1997. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Stefanovsky & Assoc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stefanovsky & Assoc.
3 devices