Techno-Path Manufacturing , Ltd.

Techno-Path Manufacturing , Ltd. — FDA 510(k) Submissions

Techno-Path Manufacturing , Ltd. has submitted 6 FDA 510(k) premarket notifications since 2013, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Multi-analyte Controls, All Kinds (assayed), Drug Mixture Control Materials, Assayed Quality Control Material For Clinical Microbiology Assays . Use the specialty filter in the sidebar to narrow results.