Tri-Tech, Inc.

Tri-Tech, Inc. — FDA 510(k) Submissions

Tri-Tech, Inc. has submitted 11 FDA 510(k) premarket notifications since 1981, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Exerciser, Measuring, Tubes, Vials, Systems, Serum Separators, Blood Collection, Kit, Screening, Urine, Ventilator, Non-continuous (respirator), Lead, Atomic Absorption . Use the specialty filter in the sidebar to narrow results.