ClearanceBrief
510(k) K971389 ยท IOR Wheelchair, Mechanical

ECLIPSE 400 MANUALLY OPERATED WHEELCAIR

ApplicantPdg Product Design Group, Inc., Vancouver, Bc, CA
DecisionSubstantially Equivalent, May 9, 1997
ReceivedApr 14, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K971389

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.