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FDA 510(k) Applications Submitted by JOHNSON & JOHNSON CONSUMER COMPANIES, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K001023
03/30/2000
FREEDOM, MODEL 4660
JOHNSON & JOHNSON CONSUMER COMPANIES, INC.
K062602
09/01/2006
BAND-AID(R) BRAND LIQUID BANDAGE
JOHNSON & JOHNSON CONSUMER COMPANIES, INC.
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