Gradipore , Ltd. is one of 147 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Gradipore , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: GRADIPLASMA LA HIGH, GRADIPLASMA LA LOW MODELS LAHP-1, LAHP-05, LALP-1, LALP-05, GRADILEIDEN V TEST
4
Total
4
Cleared
0
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.
FDA 510(k) Regulatory Record - Gradipore , Ltd.
4 devices