ClearanceBrief
510(k) K071219 ยท MVJ Devices, Measure, Antibodies To Glomerular Basement Membrane (Gbm)

ATHENA MULTI-LYTE GBM TEST SYSTEM

ApplicantZeus Scientific, Inc., Branchburg NJ, US
DecisionSubstantially Equivalent, Dec 6, 2007
ReceivedMay 2, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K071219

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.