ClearanceBrief
510(k) K062602 ยท KMF Bandage, Liquid

BAND-AID(R) BRAND LIQUID BANDAGE

ApplicantJohnson & Johnson Consumer Companies, Inc., Skillman NJ, US
DecisionSubstantially Equivalent, Dec 11, 2006
ReceivedSep 1, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K062602

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.