Medical Device Manufacturer · MX , Mexico

Artefactos DE Vidrio S.A. DE C.V. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1990

Total

Cleared

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.

Artefactos DE Vidrio S.A. DE C.V. is one of 15 FDA 510(k) medical device manufacturers from Mexico in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Artefactos DE Vidrio S.A. DE C.V.

1 devices

1-1 of 1