Medical Device Manufacturer · US , Denver , CO

Amerimed US Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1988

Total

Cleared

Denied

Amerimed US Corp. has 5 FDA 510(k) cleared medical devices. Based in Denver, US.

Historical record: 5 cleared submissions from 1988 to 1989. Primary specialty: General Hospital.

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

Amerimed US Corp. 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 - Amerimed US Corp.

5 devices

1-5 of 5