ClearanceBrief
510(k) K962219 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter

QUICKSTICK ONE STEP PREGNANCY TEST(9010)

ApplicantPhamatech, Sandiego CA, US
DecisionSubstantially Equivalent, Jul 23, 1996
ReceivedJun 10, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K962219

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.