ClearanceBrief
510(k) K240932 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

HybridTherm System

ApplicantErbe Elektromedizin GmbH, Tuebingen, DE
DecisionSubstantially Equivalent, Aug 5, 2024
ReceivedApr 5, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K240932

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.