P.T. Greenleaf is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
P.T. Greenleaf - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
P.T. Greenleaf has 2 FDA 510(k) cleared medical devices. Based in Perth, AU.
Historical record: 2 cleared submissions from 2003 to 2003. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by P.T. Greenleaf Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - P.T. Greenleaf
2 devices