General Electric Co. - FDA 510(k) Cleared Devices
254
Total
254
Cleared
0
Denied
254 devices
Cleared
Nov 19, 1976
SUPERMAX AUTOMATIC X-RAY PROCESSOR
Radiology
24d
Cleared
Oct 05, 1976
CT/N-II SCANNER SYSTEM
Radiology
15d
Cleared
Sep 10, 1976
PATIENT MONITORING SYSTEM
Cardiovascular
8d
Cleared
Aug 26, 1976
TABLE, X-RAY, RFX CLASSICAL
Radiology
8d
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