ClearanceBrief
510(k) K113063 ยท JAK System, X-Ray, Tomography, Computed

CT-GUIDE NEEDLE GUIDANCE SYSTEM

ApplicantActiviews, Ltd., Washington DC, US
DecisionSubstantially Equivalent, Nov 10, 2011
ReceivedOct 14, 2011
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K113063

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.