FDA 510(k) K140342, QCT PRO ASYNCHRONOUS CALIBRATION MODULE, CLINIQCT, by Mindways Software, Inc.

510(K) Number: K140342
Device Name: QCT PRO ASYNCHRONOUS CALIBRATION MODULE, CLINIQCT
Manufacturer: Mindways Software, Inc.
Device Classification Name: densitometer, bone
Regulation Number: 892.1170
Classification Product Code: KGI
Date Received: 02/11/2014
Decision Date: 08/29/2014
Regulation Medical Specialty: Radiology

Total pages: 1228
Fully redacted pages: 197
Content pages: 1031