Surgi-Quip Inc.U

Surgi-Quip Inc.U — FDA 510(k) Submissions

Surgi-Quip Inc.U has submitted 8 FDA 510(k) premarket notifications since 1982, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Chair, Neurosurgical, Table, Operating-room, Manual, Microscope, Surgical, Applicator, Ocular Pressure, Table, Operating-room, Ac-powered . Use the specialty filter in the sidebar to narrow results.