ClearanceBrief
510(k) K092450 ยท CZJ Igd, Antigen, Antiserum, Control

HUMAN IGD KIT FOR USE ON SPAPLUS

ApplicantThe Binding Site, Los Angeles CA, US
DecisionSubstantially Equivalent, Dec 28, 2009
ReceivedAug 10, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K092450

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.