Medical Device Manufacturer · SE , Se-103 93 Stockholm

Inomed GmbH - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2004

Total

Cleared

Denied

Inomed GmbH has 1 FDA 510(k) cleared medical devices. Based in Se-103 93 Stockholm, SE.

Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Inomed GmbH Filter by specialty or product code using the sidebar.

Inomed GmbH is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Inomed GmbH

1 devices

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