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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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