Biopsybell S.A.S. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biopsybell S.A.S. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Biopsybell S.A.S. has 3 FDA 510(k) cleared medical devices. Based in South Glastonbury, US.
Historical record: 3 cleared submissions from 2001 to 2001. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Biopsybell S.A.S. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biopsybell S.A.S.
3 devices