Medical Device Manufacturer · NL , 2596 Bt S-Gravenhage

Omnimed B.V. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1987

Total

Cleared

Denied

Omnimed B.V. has 1 FDA 510(k) cleared medical devices. Based in 2596 Bt S-Gravenhage, NL.

Historical record: 1 cleared submissions from 1987 to 1987. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Omnimed B.V. Filter by specialty or product code using the sidebar.

Omnimed B.V. is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Omnimed B.V.

1 devices

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