ClearanceBrief
510(k) K120306 ยท MED Sterilant, Medical Devices

RAPICIDE OPA-28

ApplicantMinntech Corp., Minneapolis MN, US
DecisionSubstantially Equivalent, Sep 27, 2012
ReceivedFeb 1, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K120306

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.