FDA 510(k), K170195, QuantX

FDA 510(k), K170195, QuantX

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510(K) Number: K170195
Device Name: QuantX
Manufacturer: Robert Tomek
Device Classification Name: System, Image Processing, Radiological
Regulation Number: LLZ
Classification Product Code: 01/23/2017
Date Received: 05/17/2017
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Radiology

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