Kvm Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kvm Technologies, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Kvm Technologies, Inc. has 5 FDA 510(k) cleared medical devices. Based in Houston, US.
Historical record: 5 cleared submissions from 1988 to 1993. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Kvm Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kvm Technologies, Inc.
5 devices
Cleared
Mar 09, 1993
THERAPACER 3000
Physical Medicine
119d
Cleared
Oct 12, 1988
KVM ISOTONIC FLUSH SOLUTION
Hematology
22d
Cleared
Oct 12, 1988
KVM ISOTONIC DILUENT
Hematology
22d
Cleared
Oct 12, 1988
KVM HEMOGLOBIN LYSING REAGENT
Hematology
22d
Cleared
Oct 12, 1988
KVM PREPACK HEMATOLOGY REAGENT SET
Hematology
22d