ClearanceBrief
510(k) K131236 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter

UCP PREGNANCY CASSETTE TEST, DIP/CARD STRIP, HOME PREGNANCY CASSETTE TEST, MIDSTREAM TEST AND DIP/CARD STRIP

ApplicantUcp Biosciences, Inc., San Jose CA, US
DecisionSubstantially Equivalent, Nov 7, 2013
ReceivedMay 1, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K131236

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.