Prosun International, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Prosun International, LLC - FDA 510(k) Cleared Devices
Recent clearances: ProSun sunlamp products, Luxura sunlamp products
1
Total
1
Cleared
0
Denied
Prosun International, LLC has 1 FDA 510(k) cleared medical devices. Based in Saint Petersburg, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Prosun International, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Prosun International, LLC
1 devices