Rocket of London, Ltd.

Rocket of London, Ltd. — FDA 510(k) Submissions

Rocket of London, Ltd. has submitted 3 FDA 510(k) premarket notifications since 1993, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Forceps, General & Plastic Surgery, Sound, Uterine, Light, Catheter, Fiberoptic, Glass, Ureteral . Use the specialty filter in the sidebar to narrow results.