Medical Device Manufacturer · FR , Rennes

Etiam S.A.S.U. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2013

Total

Cleared

Denied

Etiam S.A.S.U. has 1 FDA 510(k) cleared medical devices. Based in Rennes, FR.

Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Etiam S.A.S.U. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Etiam S.A.S.U.

1 devices

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