Kvm Technologies, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 5
What Kvm Technologies, Inc. makes
Kvm Technologies, Inc. manufactures isotonic diluents and flush solutions for medical use, as well as hematology reagents and hemoglobin lysing reagents. Their portfolio includes pre-packaged reagent sets for laboratory testing and a device called the Therapacer 3000, which appears to be a specialized medical instrument.
The company’s products are regulated under FDA’s 510(k) pathway, with devices classified as Class I and Class II. These products are listed in the FDA’s 510(k) clearance registry, and the company is based in the United States.
Catalogue
Kvm Isotonic Diluent Ref K883990
510(k) 510(k)Kvm Hemoglobin Lysing Reagent Ref K883991
510(k) 510(k)Therapacer 3000 Ref K925666
510(k) 510(k)Kvm Isotonic Flush Solution Ref K883989
510(k) 510(k)Kvm Prepack Hematology Reagent Set Ref K883992
510(k) 510(k)
Frequently asked questions
How many devices does Kvm Technologies, Inc. have in the registry?
The registry currently lists 5 devices for Kvm Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kvm Technologies, Inc.'s devices?
Among its 5 most recently registered devices, Kvm Technologies, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Kvm Technologies, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Kvm Technologies, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kvm Technologies, Inc. in the registry?
The most recently registered devices listed for Kvm Technologies, Inc. include KVM ISOTONIC DILUENT, KVM HEMOGLOBIN LYSING REAGENT, THERAPACER 3000 and KVM ISOTONIC FLUSH SOLUTION.