Southside Biotechnology is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Southside Biotechnology - FDA 510(k) Cleared Devices
3
Total
1
Cleared
0
Denied
Southside Biotechnology has 1 FDA 510(k) cleared medical devices. Based in North Royalton, US.
Historical record: 1 cleared submissions from 1988 to 1990. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Southside Biotechnology Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Southside Biotechnology
3 devices