FDA 510(k), K151964, Xprecia Stride Coagulation System, Xprecia System PT Controls

FDA 510(k), K151964, Xprecia Stride Coagulation System, Xprecia System PT Controls

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510(K) Number: K151964
Device Name: Xprecia Stride Coagulation System, Xprecia System PT Controls
Manufacturer: SIEMENS HEALTHCARE DIAGNOSTICS
Device Classification Name: test, time, prothrombin
Regulation Number: 864.7750
Classification Product Code: GJS
Date Received: 07/16/2015
Decision Date: 09/30/2016
Regulation Medical Specialty: Hematology
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