Palliare , Ltd.

Palliare , Ltd. — FDA 510(k) Submissions

Palliare , Ltd. has submitted 6 FDA 510(k) premarket notifications since 2020, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Insufflator, Laparoscopic, Insufflator, Automatic Carbon-dioxide For Endoscope . Use the specialty filter in the sidebar to narrow results.