Medical Device Manufacturer · FR , France

H. Girard S.A. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1986

Total

Cleared

Denied

H. Girard S.A. has 1 FDA 510(k) cleared medical devices. Based in France, FR.

Historical record: 1 cleared submissions from 1986 to 1986. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by H. Girard S.A. Filter by specialty or product code using the sidebar.

H. Girard S.A. is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - H. Girard S.A.

1 devices

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