Medical Device Manufacturer · FR , Bois Le Roi

Hennert S.A. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1995

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Hennert S.A. Ophthalmic ✕

1 devices

1-1 of 1

Cleared Aug 08, 1995

Ophthalmic · 54d