Trek Diagnostic Systems

Trek Diagnostic Systems — FDA 510(k) Submissions

Trek Diagnostic Systems has submitted 5 FDA 510(k) premarket notifications since 2011, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Manual Antimicrobial Susceptibility Test Systems, Reagent/device, Inoculum Calibration, Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems, Susceptibility Test Plate, Antifungal . Use the specialty filter in the sidebar to narrow results.