Medical Device Manufacturer · SE , Bulach

Schneider (Europe) GmbH - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1995

Total

Cleared

Denied

Schneider (Europe) GmbH has 5 FDA 510(k) cleared medical devices. Based in Bulach, SE.

Historical record: 5 cleared submissions from 1995 to 1999. Primary specialty: Cardiovascular.

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

Schneider (Europe) 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 - Schneider (Europe) GmbH

5 devices

1-5 of 5