FDA 510(k) Applications Submitted by BAYER GROUP DIAGNOSTICS

FDA 510(k) Number Submission Date Device Name Applicant
K020208 01/22/2002 GLUCOMETER ELITE DIABETES CARE SYSTEM (MODIFIED) BAYER GROUP DIAGNOSTICS
K020210 01/22/2002 GLUCOMETER DEX BLOOD GLUCOSE SYSTEM (MODIFIED) BAYER GROUP DIAGNOSTICS


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