Medical Device Manufacturer · US , Essex Junction , VT

Promedon - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2002

Total

Cleared

Denied

Promedon has 2 FDA 510(k) cleared medical devices. Based in Essex Junction, US.

Historical record: 2 cleared submissions from 2002 to 2003. Primary specialty: Gastroenterology & Urology.

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

Promedon 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 - Promedon

2 devices

1-2 of 2