ClearanceBrief
510(k) K940377 ยท HHD Pad, Menstrual, Unscented

UNSCENTED MENSTRUAL PAD TIER-1 REVIEW

ApplicantEldari, Ltd., Washington DC, US
DecisionSubstantially Equivalent, Mar 25, 1994
ReceivedJan 26, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K940377

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.