FDA 510(k), K163623, Quantra

FDA 510(k), K163623, Quantra

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510(K) Number: K163623
Device Name: Quantra
Manufacturer: HOLOGIC, INC.
Device Classification Name: system, image processing, radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 12/22/2016
Decision Date: 10/20/2017
Regulation Medical Specialty: Radiology

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