ClearanceBrief
510(k) K013678 ยท DHA System, Test, Human Chorionic Gonadotropin

VICTORCH MEDITEK'S HCG TEST CARD

ApplicantVictorch Meditek, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Dec 27, 2001
ReceivedNov 7, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K013678

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.