Medical Device Manufacturer · US , Kalamazoo , MI

Radiplast AB - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1985

Total

Cleared

Denied

Radiplast AB has 1 FDA 510(k) cleared medical devices. Based in Kalamazoo, US.

Historical record: 1 cleared submissions from 1985 to 1985. Primary specialty: Gastroenterology & Urology.

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

Radiplast AB 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 - Radiplast AB

1 devices

1-1 of 1