ClearanceBrief
510(k) K031899 ยท PSZ Devices Detecting Influenza A, B, And C Virus Antigens

QUICKVUE INFLUENZA A+B TEST

ApplicantQuidel Corp., San Diego CA, US
DecisionSubstantially Equivalent, Sep 11, 2003
ReceivedJun 4, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K031899

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.