ClearanceBrief
510(k) K233615 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

Electrosurgical Pads (GBS-Dm 1030ac, GBS-Db 1031ac, GBS-Dm 1030a, GBS-Db 1031a, GBS-Dm 1130ac, GBS-Db 1131ac, GBS-Dm 1130a, GBS-Db 1131a, GBS-Dm 1040ac, GBS-Db 1041ac, GBS-Dm 1040a, GBS-Db 1041a, GBS-Dm 1140ac, GBS-Db 1141ac, GBS-Dm 1140a, GBS-Db 1141a, GBS-Db 4030c, GBS-Db 4030, GBS-Db 4040c, GBS-D

ApplicantBaisheng Medical Co., Ltd., Jiangmen, CN
DecisionSubstantially Equivalent, Jan 8, 2024
ReceivedNov 13, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K233615

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.