Sc Hennig Enterprises Europe Srl is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Sc Hennig Enterprises Europe Srl - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Sc Hennig Enterprises Europe Srl has 1 FDA 510(k) cleared medical devices. Based in Western Australia, AU.
Historical record: 1 cleared submissions from 1999 to 1999. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Sc Hennig Enterprises Europe Srl Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sc Hennig Enterprises Europe Srl
1 devices