ClearanceBrief
510(k) K926173 ยท JWX Kit, Screening, Staphylococcus Aureus

STAPH-A-LEX(TM) SYSTEM

ApplicantTrinity Laboratories, Inc., Raleigh NC, US
DecisionSubstantially Equivalent, Aug 10, 1993
ReceivedDec 8, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K926173

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.