Medical Device Manufacturer · FR , Chartres Cedex

Luneau Ophtalmologie SA - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1991

Total

Cleared

Denied

Luneau Ophtalmologie SA has 3 FDA 510(k) cleared medical devices. Based in Chartres Cedex, FR.

Historical record: 3 cleared submissions from 1991 to 1992. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Luneau Ophtalmologie SA Filter by specialty or product code using the sidebar.

Luneau Ophtalmologie SA 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 - Luneau Ophtalmologie SA

3 devices

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