FDA 510(k), K062187, BETACHEK GLUCOSE TEST

FDA 510(k), K062187, BETACHEK GLUCOSE TEST

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510(K) Number: K062187
Device Name: BETACHEK GLUCOSE TEST
Manufacturer:
Device Classification Name: System, Test, Blood Glucose, Over The Counter
Regulation Number: 862.1345
Classification Product Code: NBW
Date Received: 08/01/2006
Decision Date: 03/24/2009
Regulation Medical Specialty: Clinical Chemistry
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