George Courey, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
George Courey, Inc. has 2 FDA 510(k) cleared medical devices. Based in Laval, CA.
Latest FDA clearance: Jun 2025. Active since 2024. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by George Courey, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by George Courey, Inc.
2 devices