Sechrist Industries, Inc.

Sechrist Industries, Inc. — FDA 510(k) Submissions

Sechrist Industries, Inc. has submitted 23 FDA 510(k) premarket notifications since 1978, of which 22 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Ventilator, Continuous, Facility Use, Chamber, Hyperbaric, Mixer, Breathing Gases, Anesthesia Inhalation, Monitor, Airway Pressure (includes Gauge And/or Alarm), Tubing, Fluid Delivery . Use the specialty filter in the sidebar to narrow results.