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FDA 510(k) Applications Submitted by CATHY PETERS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090413
02/18/2009
A1CNOW+ (10 TEST KIT, PROFESSIONAL USE) MODEL 3024, A1CNOW+(20 TEST KIT, PROFESSIONAL USE) MODEL 3021, A1CNOW SELF CHEC
BAYER HEALTHCARE, LLC
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