Medical Device Manufacturer · US , Denton , TX

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

1 submissions · 1 cleared · Since 2005

Total

Cleared

Denied

Etiam, S.A. has 1 FDA 510(k) cleared medical devices. Based in Denton, US.

Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Radiology.

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

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

1 devices

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