Medical Device Manufacturer · FR , Chartres Cedex

Luneau Gynecologie SA - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2000

Total

Cleared

Denied

Luneau Gynecologie SA has 1 FDA 510(k) cleared medical devices. Based in Chartres Cedex, FR.

Historical record: 1 cleared submissions from 2000 to 2000. Primary specialty: Obstetrics & Gynecology.

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

Luneau Gynecologie 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 Gynecologie SA

1 devices

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