Level 1 Technologies, Inc.

Level 1 Technologies, Inc. — FDA 510(k) Submissions

Level 1 Technologies, Inc. has submitted 5 FDA 510(k) premarket notifications since 1987, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Urological, Warmer, Thermal, Infusion Fluid, Apparatus, Suction, Single Patient Use, Portable, Nonpowered, Set, Administration, Intravascular, Apparatus, Autotransfusion . Use the specialty filter in the sidebar to narrow results.