Artefactos DE Vidrio S.A. DE C.V. is one of 9 FDA 510(k) medical device manufacturers from Mexico in the dataset, ranked by real submission volume.
Artefactos DE Vidrio S.A. DE C.V. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Artefactos DE Vidrio S.A. DE C.V. has 1 FDA 510(k) cleared medical devices. Based in Mexico, MX.
Historical record: 1 cleared submissions from 1990 to 1990. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Artefactos DE Vidrio S.A. DE C.V. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Artefactos DE Vidrio S.A. DE C.V.
1 devices