Voroba Technologies Assoc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Voroba Technologies Assoc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Voroba Technologies Assoc. has 2 FDA 510(k) cleared medical devices. Based in Minnetonka, US.
Historical record: 2 cleared submissions from 1986 to 1986. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Voroba Technologies Assoc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Voroba Technologies Assoc.
2 devices