Medical Device Manufacturer · NO , Horten

Fimreite Software AS - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2010

Total

Cleared

Denied

Fimreite Software AS has 1 FDA 510(k) cleared medical devices. Based in Horten, NO.

Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Fimreite Software AS Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Fimreite Software AS

1 devices

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