FDA 510(k), K141929, ACCU-CHEK CONNECT DIABETES MANAGEMENT APP

FDA 510(k), K141929, ACCU-CHEK CONNECT DIABETES MANAGEMENT APP

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510(K) Number: K141929
Device Name: ACCU-CHEK CONNECT DIABETES MANAGEMENT APP
Manufacturer: ROCHE DIAGNOSTICS CORPORATION
Device Classification Name: calculator, drug dose
Regulation Number: 868.1890
Classification Product Code: NDC
Date Received: 07/16/2014
Decision Date: 03/16/2015
Regulation Medical Specialty: Anesthesiology
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