B.V. Intl. S.A. is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
B.V. Intl. S.A. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
B.V. Intl. S.A. has 1 FDA 510(k) cleared medical devices. Based in Clermont-Ferrand, FR.
Historical record: 1 cleared submissions from 1996 to 1996. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by B.V. Intl. S.A. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - B.V. Intl. S.A.
1 devices