ClearanceBrief
510(k) K120116 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

SERF ABLATION SYSTEM SERF ABLATION NEEDLE

ApplicantThermedical, Philedelphia PA, US
DecisionSubstantially Equivalent, Oct 1, 2012
ReceivedJan 13, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K120116

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.