ClearanceBrief
510(k) K032997 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function

MODIFICATION TO: HORIZON 9000WS

ApplicantMennen Medical , Ltd., Yavne, IL
DecisionSubstantially Equivalent, Oct 15, 2003
ReceivedSep 25, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K032997

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.