Urological Assoc. of Grand Island, P.C. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Urological Assoc. of Grand Island, P.C. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Urological Assoc. of Grand Island, P.C. has 1 FDA 510(k) cleared medical devices. Based in Grand Island, US.
Historical record: 1 cleared submissions from 1989 to 1989. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Urological Assoc. of Grand Island, P.C. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Urological Assoc. of Grand Island, P.C.
1 devices