PAJUNK GmbH Medizintechnologie

PAJUNK GmbH Medizintechnologie — FDA 510(k) Submissions

PAJUNK GmbH Medizintechnologie has submitted 44 FDA 510(k) premarket notifications since 2006, of which 44 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Needle, Conduction, Anesthetic (w/wo Introducer), Anesthesia Conduction Kit, Catheter, Conduction, Anesthetic, Neurological Stereotaxic Instrument, Laparoscope, General & Plastic Surgery . Use the specialty filter in the sidebar to narrow results.