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Spectrum X-Ray Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K933134SPECTRUM DG-P7000 PEDIATRIC CRADLEOctober 7, 1993
K931563SPECTRUM MARK I SPECIAL PROCEDURES TABLEAugust 23, 1993
K870707PENTAMAX 1 MODEL B TABLE SYSTEMMay 14, 1987
K834494SPECTRUM X-RAY CORPFebruary 21, 1984
K840463DIGITAL CRADLEFebruary 21, 1984
K827450SIMPLAMATIC IIIMay 19, 1982
K813561SPECTRUM PEDIATRIC CARDLE TABLEJanuary 29, 1982
K791812SPECTRUM EMERGENCY & TRAUMA TABLE SYSTEMNovember 5, 1979
K791811SPECTRUM AUTOMATIC CHEST UNIT MODEL COctober 26, 1979