Cannon U.S.A., Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Cannon U.S.A., Inc. has 2 FDA 510(k) cleared medical devices. Based in Lake Success, US.
Historical record: 2 cleared submissions from 1994 to 1996. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Cannon U.S.A., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Cannon U.S.A., Inc.
2 devices