Amsino Intl., Inc.

Amsino Intl., Inc. — FDA 510(k) Submissions

Amsino Intl., Inc. has submitted 9 FDA 510(k) premarket notifications since 1995, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Collector, Urine, (and Accessories) For Indwelling Catheter, System, Irrigation, Urological, Spatula, Cervical, Cytological, Speculum, Vaginal, Nonmetal, Set, Administration, Intravascular . Use the specialty filter in the sidebar to narrow results.