ClearanceBrief
510(k) K123567 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter

FIRST RESPONSE GOLD DIGITAL PREGNANCY TEST

ApplicantChurch & Dwight Co., Inc., Princeton NJ, US
DecisionSubstantially Equivalent, Sep 10, 2013
ReceivedNov 20, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K123567

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.