Medical Device Manufacturer · AU , Pyrmont

Gradipore , Ltd. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1990

Total

Cleared

Denied

Gradipore , Ltd. has 4 FDA 510(k) cleared medical devices. Based in Pyrmont, AU.

Historical record: 4 cleared submissions from 1990 to 2000. Primary specialty: Hematology.

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

Gradipore , Ltd. is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Gradipore , Ltd.

4 devices

1-4 of 4