Clarus Medical Systems, Inc.

Clarus Medical Systems, Inc. — FDA 510(k) Submissions

Clarus Medical Systems, Inc. has submitted 22 FDA 510(k) premarket notifications since 1992, of which 20 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Endoscope, Neurological, Arthroscope, Catheter, Cholangiography, Instrument, Microsurgical, Otoscope . Use the specialty filter in the sidebar to narrow results.