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Kvm Technologies, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K925666THERAPACER 3000March 9, 1993
K883990KVM ISOTONIC DILUENTOctober 12, 1988
K883991KVM HEMOGLOBIN LYSING REAGENTOctober 12, 1988
K883989KVM ISOTONIC FLUSH SOLUTIONOctober 12, 1988
K883992KVM PREPACK HEMATOLOGY REAGENT SETOctober 12, 1988