V. Mueller O.V. Baxter Healthcare Corp.

V. Mueller O.V. Baxter Healthcare Corp. — FDA 510(k) Submissions

V. Mueller O.V. Baxter Healthcare Corp. has submitted 41 FDA 510(k) premarket notifications since 1976, of which 41 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Cystoscope And Accessories, Flexible/rigid, Scissors, Ophthalmic, Knife, Ophthalmic, Resectoscope, Working Element, Surgical Instruments, G-u, Manual (and Accessories) . Use the specialty filter in the sidebar to narrow results.