Kvm Technologies, Inc.

Kvm Technologies, Inc. — FDA 510(k) Submissions

Kvm Technologies, Inc. has submitted 5 FDA 510(k) premarket notifications since 1988, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Diluent, Blood Cell, Products, Red-cell Lysing Products, Cyanomethemoglobin, Exerciser, Powered . Use the specialty filter in the sidebar to narrow results.