ClearanceBrief
510(k) K984493 ยท IOR Wheelchair, Mechanical

MAXXIM; MAXXIM HD

ApplicantMajor Mobility Products, Inc., Houston TX, US
DecisionSubstantially Equivalent, Jan 8, 1999
ReceivedDec 17, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K984493

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.