ClearanceBrief
510(k) K950903 ยท IOR Wheelchair, Mechanical

ORTHOFAB WHEELCHAIR ULTIMA (RIGID FRAME MANUAL WHEELCHAIR)

ApplicantOrthofab, Inc., Quebec, Quebec, CA
DecisionSubstantially Equivalent, Apr 5, 1995
ReceivedFeb 28, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K950903

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.