ClearanceBrief
510(k) K042341 ยท NEU Marker, Radiographic, Implantable

ULTRACLIP II US

ApplicantInrad, Kentwood MI, US
DecisionSubstantially Equivalent, Sep 20, 2004
ReceivedAug 30, 2004
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K042341

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.