ClearanceBrief
510(k) K001890 ยท IOR Wheelchair, Mechanical

SHERPA/KODIAK CUB MOBILITY SYSTEM (MANUAL WHEELCHAIR)

ApplicantOtto Bock Orthopaedische Industrie, Kg., Minneapolis MN, US
DecisionSubstantially Equivalent, Jul 24, 2000
ReceivedJun 21, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K001890

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.