Medical Device Manufacturer · FR , Nantes

Adiatec SA - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2004

Total

Cleared

Denied

Adiatec SA has 1 FDA 510(k) cleared medical devices. Based in Nantes, FR.

Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: Immunology.

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

Adiatec 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 - Adiatec SA

1 devices

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