ClearanceBrief
510(k) K191601 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

Valleylab FT10 Electrosurgical Platform

ApplicantCovidien, Boulder CO, US
DecisionSubstantially Equivalent, Jul 12, 2019
ReceivedJun 17, 2019
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K191601

DateFirm and productCodeLinked 510(k)
Jan 3, 2024Covidien
Covidien Valleylab FT10, FT Series Energy Platform, REF: VLFT10GEN, DLVLFT10GEN, VLFT10GENZD
Open, Classified
GEINone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.