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Zeus Technologies

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K840012INDIRECT FLUORESCENT ANTIBODY MYCOFebruary 27, 1984
K831026INDIRECT FLUORESCENT ANTIBODY REAGENTSJune 22, 1983
K830783VERI-STAPHApril 8, 1983
K822859DIRECT FA CONJUGATE FOR LEGIONELLA SPPFebruary 16, 1983