Rocket Medical Plc

Rocket Medical Plc — FDA 510(k) Submissions

Rocket Medical Plc has submitted 19 FDA 510(k) premarket notifications since 1996, of which 16 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Apparatus, Suction, Patient Care, Peritoneal, Drainage Catheter For Refractory Ascites, Long-term Indwelling, Needle, Assisted Reproduction, Catheter, Assisted Reproduction, Wire, Guide, Catheter . Use the specialty filter in the sidebar to narrow results.