ClearanceBrief
510(k) K761339 ยท IZZ Table, Radiographic, Non-Tilting, Powered

RADIAL TRAVEL SPEC. PROCEDURES TABLE

ApplicantXre Corp., Walker MI, US
DecisionSubstantially Equivalent, Jan 5, 1977
ReceivedDec 27, 1976
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K761339

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.