General Electric Co. - FDA 510(k) Cleared Devices
Recent clearances: GE VEO RECONSTRUCTION OPTION, GE LUNAR FRAX 10-YEAR FRACTURE RISK SOFTWARE OPTION, GE VIVID E9 ULTRASOUND
254
Total
254
Cleared
0
Denied
FDA 510(k) Regulatory Record - General Electric Co. Neurology ✕
1 devices