Graoipore , Ltd. is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Graoipore , Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Graoipore , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Pyrmont 2009 Australia, AU.
Historical record: 1 cleared submissions from 1993 to 1993. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Graoipore , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Graoipore , Ltd.
1 devices