Intertech Resources, Inc.

Intertech Resources, Inc. — FDA 510(k) Submissions

Intertech Resources, Inc. has submitted 29 FDA 510(k) premarket notifications since 1987, of which 27 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Ventilator, Emergency, Manual (resuscitator), Condenser, Heat And Moisture (artificial Nose), Filter, Bacterial, Breathing-circuit, Resuscitator, Manual, Non Self-inflating, Set, Tubing And Support, Ventilator (w Harness) . Use the specialty filter in the sidebar to narrow results.