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General X-Ray, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K800998ATLAS-S X-RAY SYSTEM W/KETROMAT GEN.May 28, 1980
K790451X-RAY UNITS, GX-101, UCIS-510 AND GX-111March 28, 1979
K790512PORTABLE X-RAY UNITMarch 26, 1979
K790511MOBILE X-RAY UNITMarch 26, 1979
K790392510 CARBINETTE X-RAY UNITMarch 26, 1979
K790393PORTABLE X-RAY UNIT, MATRIX S GX-101March 26, 1979
K790443PORTABLE X-RAY UNITMarch 26, 1979
K781975MOBILE CARRIERDecember 4, 1978
K781976MOBILE X-RAY UNITDecember 4, 1978
K781675X-RAY COLLIMATORDecember 4, 1978
K781676X-RAY STAND, PORTABLEOctober 17, 1978
K781590PORTABLE X-RAY UNITOctober 3, 1978
K781030X-RAY UNIT, PORTABLE GX-101 AECJuly 17, 1978
K780963X-RAY SYSTEMJune 27, 1978