Medical Device Manufacturer · US , Temecula , CA

Nemectron GmbH - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1994

Total

Cleared

Denied

Nemectron GmbH has 2 FDA 510(k) cleared medical devices. Based in Temecula, US.

Historical record: 2 cleared submissions from 1994 to 1994. Primary specialty: Neurology.

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

Nemectron GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Nemectron GmbH

2 devices

1-2 of 2