Enteric Medical Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Enteric Medical Technologies - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Enteric Medical Technologies has 2 FDA 510(k) cleared medical devices. Based in Foster City, US.
Historical record: 2 cleared submissions from 2000 to 2002. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Enteric Medical Technologies Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Enteric Medical Technologies
2 devices