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FDA 510(k), K140342, QCT PRO ASYNCHRONOUS CALIBRATION MODULE, CLINIQCT
FDA 510(k), K140342, QCT PRO ASYNCHRONOUS CALIBRATION MODULE, CLINIQCT
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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
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
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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