ClearanceBrief
510(k) K945548 ยท KZE Injector, Fluid, Non-Electrically Powered

MEDIVAX

ApplicantVitajet Corp., Laguna Hills CA, US
DecisionSubstantially Equivalent, Nov 20, 1995
ReceivedNov 14, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K945548

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.