ClearanceBrief
510(k) K181389 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

Valleylab FT10 Energy Platform, Valleylab FX8 FX Series Energy Platform

ApplicantCovidien, Boulder CO, US
DecisionSubstantially Equivalent, Jun 19, 2018
ReceivedMay 25, 2018
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K181389

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.