Valleylab, Inc.
Valleylab, Inc. — FDA 510(k) Submissions
Valleylab, Inc. has submitted 94 FDA 510(k) premarket notifications since 1976, of which 93 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Electrosurgical, Cutting & Coagulation & Accessories, Instrument, Ultrasonic Surgical, Pump, Infusion, Set, Administration, Intravascular, Electrocautery, Gynecologic (and Accessories) . Use the specialty filter in the sidebar to narrow results.
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