Medical Device Manufacturer · IT , Scanzorosciate (Bg)

Eurotec, S.R.L. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1997

Total

Cleared

Denied

Eurotec, S.R.L. has 1 FDA 510(k) cleared medical devices. Based in Scanzorosciate (Bg), IT.

Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Eurotec, S.R.L.

1 devices

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