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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