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.
510(k) submissions have been managed by Emergo by UL as regulatory consultant.
2 devices