Maxtec, LLC

Maxtec, LLC — FDA 510(k) Submissions

Maxtec, LLC has submitted 6 FDA 510(k) premarket notifications since 2011, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Analyzer, Gas, Oxygen, Gaseous-phase, Mixer, Breathing Gases, Anesthesia Inhalation, Analyzer, Gas, Carbon-dioxide, Gaseous-phase . Use the specialty filter in the sidebar to narrow results.