Epocal, Inc.

Epocal, Inc. — FDA 510(k) Submissions

Epocal, Inc. has submitted 7 FDA 510(k) premarket notifications since 2006, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Glucose Oxidase, Glucose, Electrode, Ion Specific, Potassium, Acid, Lactic, Enzymatic Method, Electrode, Ion Based, Enzymatic, Creatinine, Electrode, Ion Specific, Urea Nitrogen . Use the specialty filter in the sidebar to narrow results.