V-Tech, Inc.

V-Tech, Inc. — FDA 510(k) Submissions

V-Tech, Inc. has submitted 22 FDA 510(k) premarket notifications since 1982, of which 22 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Visual, Pregnancy Hcg, Prescription Use, Enzyme Immunoassay, Opiates, Radioimmunoassay, Cocaine Metabolite, Enzyme Immunoassay, Amphetamine, Enzyme Immunoassay, Cannabinoids . Use the specialty filter in the sidebar to narrow results.