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Kvm Technologies, Inc.

FDA Regulatory Profile

Kvm Technologies, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 9, 1993.

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
K883989KVM ISOTONIC FLUSH SOLUTIONOctober 12, 1988
K883992KVM PREPACK HEMATOLOGY REAGENT SETOctober 12, 1988
K883991KVM HEMOGLOBIN LYSING REAGENTOctober 12, 1988

FDA data resources