FDA 510(k) K162513, Arterys Software v2.0, by Arterys, Inc.

510(K) Number: K162513
Device Name: Arterys Software v2.0
Manufacturer: Arterys, Inc.
Device Classification Name: System, Image Processing, Radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 09/08/2016
Decision Date: 10/28/2016
Regulation Medical Specialty: Radiology