Hsiner Co., Ltd.

Hsiner Co., Ltd. — FDA 510(k) Submissions

Hsiner Co., Ltd. has submitted 7 FDA 510(k) premarket notifications since 2005, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Nebulizer (direct Patient Interface), Ventilator, Continuous, Facility Use, Ventilator, Emergency, Manual (resuscitator), Ventilator, Non-continuous (respirator), Filter, Bacterial, Breathing-circuit . Use the specialty filter in the sidebar to narrow results.