Mid Tech, Inc.

Mid Tech, Inc. — FDA 510(k) Submissions

Mid Tech, Inc. has submitted 5 FDA 510(k) premarket notifications since 1977, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Ph Buffer, Nadh Oxidation/nad Reduction, Alt/sgpt, Multi-analyte Controls, All Kinds (assayed), Glucose Oxidase, Glucose . Use the specialty filter in the sidebar to narrow results.