ClearanceBrief
Company ยท US

Kvm Technologies, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1988 to 1993. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GIFDiluent, Blood Cell2
BXBExerciser, Powered1
GGKProducts, Red-Cell Lysing Products1
GKKCyanomethemoglobin1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 9, 1993K925666THERAPACER 3000
Kvm Technologies, Inc.
BXB
Oct 12, 1988K883992KVM PREPACK HEMATOLOGY REAGENT SET
Kvm Technologies, Inc.
GKK
Oct 12, 1988K883991KVM HEMOGLOBIN LYSING REAGENT
Kvm Technologies, Inc.
GGK
Oct 12, 1988K883990KVM ISOTONIC DILUENT
Kvm Technologies, Inc.
GIF
Oct 12, 1988K883989KVM ISOTONIC FLUSH SOLUTION
Kvm Technologies, Inc.
GIF

Latest recalls

DateFirm and productCodeLinked 510(k)
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