ClearanceBrief
510(k) K060819 ยท KZE Injector, Fluid, Non-Electrically Powered

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ApplicantMedical House Products Limited, Sheffield, GB
DecisionSubstantially Equivalent, Jun 16, 2006
ReceivedMar 27, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K060819

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.