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. Obstetrics & Gynecology ✕
5 devices
Cleared
Jun 02, 1986
5 MHZ INTRACAVITARY PROBE, MODEL H4222V
Obstetrics & Gynecology
131d
Cleared
Dec 18, 1985
5.0 MHZ INTRACAVITARY SECTOR PROBE
Obstetrics & Gynecology
104d
Cleared
Mar 13, 1981
DATASON DB ULTRASOUND IMAGING SYSTEM
Obstetrics & Gynecology
36d
Cleared
Aug 04, 1977
ARTIUS SYSTEM
Obstetrics & Gynecology
41d
Cleared
Dec 16, 1976
V.I. OCTOSON ULTRASONIC SYSTEM
Obstetrics & Gynecology
59d