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FDA 510(k)

Electrosurgical Pads

K-Number: K251235 · 2025-06-19

ApplicantBaisheng Medical Co., Ltd.
Decision Date2025-06-19
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Electrosurgical Pads is a medical device manufactured by Baisheng Medical Co., Ltd.. It received FDA 510(k) clearance on 2025-06-19 under approval number K251235. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Electrosurgical Pads?

Electrosurgical Pads is a medical device that received FDA 510(k) clearance on 2025-06-19. It is manufactured by Baisheng Medical Co., Ltd.. The 510(k) number is K251235.

When was Electrosurgical Pads approved by the FDA?

Electrosurgical Pads received FDA 510(k) clearance on 2025-06-19, under approval number K251235.

What company makes Electrosurgical Pads?

Electrosurgical Pads is manufactured by Baisheng Medical Co., Ltd..

What is the FDA product code for Electrosurgical Pads?

The FDA product code for Electrosurgical Pads is GEI.

Other Devices by Baisheng Medical Co., Ltd.

K162034OBS Electrosurgical Generator (Model: OBS-350A) K221815Electrosurgical Pencil (OBS-Db, OBS-Dr, OBS-Dc, OBS-Df, OBS-Di, OBS-De); Electrosurgical Pencil (OBS-Dt, OBS-Dd, OBS-Ds, OBS-Dl, OBS-Da) K233615Electrosurgical 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-Db 4040, GBS-Dm 1030bc, GBS-Db 1031bc, GBS-Dm 1030b, GBS-Db 1031b, GBS-Dm 1130bc, GBS-Db 1131bc, GBS-Dm 1130b, GBS-Db 1131b, GBS-Dm 1030nc, GBS-Db 1031nc, GBS-Dm 1030n, GBS-Db 1031n, GBS-Dm 1 K250841Electrotherapy Electrodes

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Official Source

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