Triton Technology, Inc.

Triton Technology, Inc. — FDA 510(k) Submissions

Triton Technology, Inc. has submitted 4 FDA 510(k) premarket notifications since 1988, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Instrument, Biopsy, Suction, Probe, Blood-flow, Extravascular, Trap, Sterile Specimen . Use the specialty filter in the sidebar to narrow results.