Medical Device Manufacturer · US , Ventura , CA

Biopool Intl., Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1998

Total

Cleared

Denied

Biopool Intl., Inc. has 4 FDA 510(k) cleared medical devices. Based in Ventura, US.

Historical record: 4 cleared submissions from 1998 to 2001. Primary specialty: Hematology.

Browse the FDA 510(k) cleared devices submitted by Biopool Intl., Inc. Filter by specialty or product code using the sidebar.

Biopool Intl., Inc. 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 - Biopool Intl., Inc.

4 devices

1-4 of 4