ClearanceBrief
510(k) K882364 ยท HHD Pad, Menstrual, Unscented

KOTEX LIGHTDAYS LONGS DEODORANT & REG. PANTILINERS

ApplicantKimberly-Clark Corp., Washington DC, US
DecisionSubstantially Equivalent, Aug 2, 1988
ReceivedJun 8, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K882364

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.