ClearanceBrief
510(k) K071591 ยท PSZ Devices Detecting Influenza A, B, And C Virus Antigens

RAMP INFLUENZA A/B ASSAY

ApplicantResponse Biomedical Corp., Burnaby, British Columbia, CA
DecisionSubstantially Equivalent, Apr 16, 2008
ReceivedJun 11, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K071591

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.