ClearanceBrief
510(k) K262720 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

SP Electrocautery Device (SP18 Max);SP Electrocautery Device (SP20 Max)

ApplicantSingle Pass, Inc., Lake Forest CA, US
DecisionSubstantially Equivalent, Oct 26, 2026
ReceivedJul 31, 2026
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K262720

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.