ClearanceBrief
510(k) K990139 ยท IOR Wheelchair, Mechanical

KENSTONE

ApplicantKenda USA, Reynoldsburg OH, US
DecisionSubstantially Equivalent, Apr 29, 1999
ReceivedJan 19, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K990139

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.