Medical Device Manufacturer · FR , J.Rousseau Oyonnax,France

Lunettes Bondet - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1993
1
Total
1
Cleared
0
Denied

Lunettes Bondet has 1 FDA 510(k) cleared medical devices. Based in J.Rousseau Oyonnax,France, FR.

Historical record: 1 cleared submissions from 1993 to 1993. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Lunettes Bondet Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Lunettes Bondet

1 devices
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