ClearanceBrief
510(k) K021866 ยท IOR Wheelchair, Mechanical

KARMA 800 SERIES MANUAL WHEELCHAIR

ApplicantVestil Manufacturing Corp., Angola IN, US
DecisionSubstantially Equivalent, Jun 14, 2002
ReceivedJun 6, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K021866

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.