Clinical Laserthermia Systems, AB

Clinical Laserthermia Systems, AB — FDA 510(k) Submissions

Clinical Laserthermia Systems, AB has submitted 6 FDA 510(k) premarket notifications since 2015, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Powered Laser Surgical Instrument, Neurosurgical Laser With Mr Thermography . Use the specialty filter in the sidebar to narrow results.