Bovie Medical Corporation Dba Apyx Medical Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bovie Medical Corporation Dba Apyx Medical Corporation - FDA 510(k) C...
Recent clearances: Apyx Helium Plasma Generator (APYX-200H/P, APYX-JS3/RS3), Apyx Plasma/RF Handpiece
2
Total
2
Cleared
0
Denied
Bovie Medical Corporation Dba Apyx Medical Corporation has 2 FDA 510(k) cleared medical devices. Based in Clearwater, US.
Historical record: 2 cleared submissions from 2019 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Bovie Medical Corporation Dba Apyx Medical Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Bovie Medical Corporation Dba Apyx Medical Corporation
2 devices