ClearanceBrief
510(k) K864561 ยท KZE Injector, Fluid, Non-Electrically Powered

DERATA MEDI-JECTOR IV

ApplicantDerata Corp., Minneapolis MN, US
DecisionSubstantially Equivalent, Feb 19, 1987
ReceivedNov 19, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K864561

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.