Grupo Industrial Supertex S.A. DE C.V. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Grupo Industrial Supertex S.A. DE C.V. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Grupo Industrial Supertex S.A. DE C.V. has 1 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 1 cleared submissions from 1989 to 1989. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Grupo Industrial Supertex S.A. DE C.V. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Grupo Industrial Supertex S.A. DE C.V.
1 devices