Kelleher Corp.

Kelleher Corp. — FDA 510(k) Submissions

Kelleher Corp. has submitted 94 FDA 510(k) premarket notifications since 1982, of which 94 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laryngoscope, Nasopharyngoscope, Knife, Ent, Source, Carrier, Fiberoptic Light, Chair, Surgical, Ac-powered, Forceps, Biopsy, Bronchoscope (rigid) . Use the specialty filter in the sidebar to narrow results.