ClearanceBrief
510(k) K951005 ยท IZQ Injector, Contrast Medium, Automatic

KENEX INJECTOR HEAD SUPPORT (AS EXHIBIT 2)

ApplicantKenex , Ltd., England, GB
DecisionSubstantially Equivalent, May 4, 1995
ReceivedFeb 15, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K951005

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.