ClearanceBrief
510(k) K240999 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

Legend X Applicator VO

ApplicantPollogen, Ltd., Tel Aviv, IL
DecisionSubstantially Equivalent, May 8, 2024
ReceivedApr 11, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K240999

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.