Teco Diagnostics, Inc.

Teco Diagnostics, Inc. — FDA 510(k) Submissions

Teco Diagnostics, Inc. has submitted 4 FDA 510(k) premarket notifications since 2016, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Enzymatic Method, Creatinine, Method, Enzymatic, Glucose (urinary, Non-quantitative), Enzymatic, Carbon-dioxide . Use the specialty filter in the sidebar to narrow results.