ClearanceBrief
510(k) K180288 ยท PSZ Devices Detecting Influenza A, B, And C Virus Antigens

QuickVue Influenza A+B

ApplicantQuidel Corporation, San Diego CA, US
DecisionSubstantially Equivalent, Feb 13, 2018
ReceivedFeb 1, 2018
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K180288

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.