ClearanceBrief
510(k) K232809 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

Cross Vascular RF Generator and Footswitch (optional accessory)

ApplicantCross Vascular, Inc., Solana Beach CA, US
DecisionSubstantially Equivalent, Oct 12, 2023
ReceivedSep 12, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232809

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.