Medical Device Manufacturer · US , Irvine , CA

Asclepion-Meditec AG - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2000

Total

Cleared

Denied

Asclepion-Meditec AG has 5 FDA 510(k) cleared medical devices. Based in Irvine, US.

Historical record: 5 cleared submissions from 2000 to 2002. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Asclepion-Meditec AG Filter by specialty or product code using the sidebar.

Asclepion-Meditec AG 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 - Asclepion-Meditec AG

5 devices

1-5 of 5