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FDA 510(k) K141389, SAPPHIRE INFUSION PUMP, by Q Core Medical , Ltd.

FDA 510(k) K141389, SAPPHIRE INFUSION PUMP, by Q Core Medical , Ltd.

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510(K) Number: K141389
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: 05/27/2014
Decision Date: 12/11/2014
Regulation Medical Specialty: General Hospital
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