FDA 510(k), K161631, MAMMI

FDA 510(k), K161631, MAMMI

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510(K) Number: K161631
Device Name: MAMMI
Manufacturer: GENERAL EQUIPMENT FOR MEDICAL IMAGING
Device Classification Name: system, tomography, computed, emission
Regulation Number: 892.1200
Classification Product Code: KPS
Date Received: 06/13/2016
Decision Date: 07/28/2016
Regulation Medical Specialty: Radiology
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