FDA 510(k), K192872, ulrichINJECT CT Motion

FDA 510(k), K192872, ulrichINJECT CT Motion

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510(K) Number: K192872
Device Name: ulrichINJECT CT Motion
Manufacturer: Sven Erdmann
Device Classification Name: Injector, Contrast Medium, Automatic
Regulation Number: IZQ
Classification Product Code: 10/08/2019
Date Received: 07/02/2020
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital

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