FDA 510(k), K161667, Sapphire Infusion Pump

FDA 510(k), K161667, Sapphire Infusion Pump

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510(K) Number: K161667
Device Name: Sapphire Infusion Pump
Manufacturer: Q Core Medical Ltd.
Device Classification Name: pump, infusion
Regulation Number: 880.5725
Classification Product Code: FRN
Date Received: 06/16/2016
Decision Date: 03/27/2017
Regulation Medical Specialty: General Hospital

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