Rapid Medical , Ltd.

Rapid Medical , Ltd. — FDA 510(k) Submissions

Rapid Medical , Ltd. has submitted 9 FDA 510(k) premarket notifications since 2019, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Thrombus Retriever, Guide, Wire, Catheter, Neurovasculature, Temporary Coil Embolization Assist Device, Temporary Embolization Assist Device, Peripheral . Use the specialty filter in the sidebar to narrow results.