ClearanceBrief
510(k) K963817 ยท IPL Wheelchair, Standup

LEVO MOBIL LCM

ApplicantLevo USA, Dottikon, CH
DecisionSubstantially Equivalent, Dec 23, 1997
ReceivedSep 23, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K963817

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.