Argon Medical Devices, Inc.

Argon Medical Devices, Inc. — FDA 510(k) Submissions

Argon Medical Devices, Inc. has submitted 20 FDA 510(k) premarket notifications since 2007, of which 20 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Introducer, Catheter, Device, Percutaneous Retrieval, Peripheral Mechanical Thrombectomy With Aspiration, Catheter, Continuous Flush, Wire, Guide, Catheter . Use the specialty filter in the sidebar to narrow results.