ClearanceBrief
510(k) K140763 ยท FDI Snare, Flexible

MONOFILAMENT POLYPECTOMY SNARE

ApplicantUnited States Endoscopy, Mentor OH, US
DecisionSubstantially Equivalent, Apr 24, 2014
ReceivedMar 27, 2014
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K140763

DateFirm and productCodeLinked 510(k)
Oct 1, 2015US Endoscopy Group Inc
Histolock Resection Device, US Endoscopy. An electrosurgical device designed to be used to endoscopically grasp, dissect and transect tissue during gastrointestinal endoscopic procedures.
Terminated
FDINone listed

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