ClearanceBrief
510(k) K041748 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter

AZOG, INC. HCG ONE-STEP URINE HOME PREGNANCY TEST (DIP STICK, CASSETTE AND MIDSTREAM)

ApplicantAzog, Inc., Phillipsburg NJ, US
DecisionSubstantially Equivalent, Aug 9, 2004
ReceivedJun 29, 2004
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K041748

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.