ClearanceBrief
510(k) K150735 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

Force TriVerse Electrosugical Device, Holster, 10-foot, Force TriVerse Electrosurgical Device, Holster, 15-foot

ApplicantCovidien, Boulder CO, US
DecisionSubstantially Equivalent, Aug 4, 2015
ReceivedMar 20, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K150735

DateFirm and productCodeLinked 510(k)
Feb 25, 2020Covidien Llc
Covidien Force TriVerse Electrosurgical Devices, Product numbers FT3000 and FT3000DB, UDI 10884524000084 20884524000081; 10884524001937 20884524001934
Terminated
GEINone listed
Feb 15, 2019Covidien, PLC
Covidien Force TriVerse electrosurgical device 10 cord-Intended as electrosurgical energy to cut and/or coagulate tissue. Product Usage: Single-use device intended for use in open procedures (such a
Terminated
GEINone listed

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