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FDA 510(k)

Electrosurgical Pads

K-Number: K251235 · 2025-06-19

Decision Date2025-06-19
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Electrosurgical Pads is the device name listed in this FDA 510(k) record. The listed applicant is Baisheng Medical Co., Ltd.. It received FDA 510(k) clearance on 2025-06-19 under 510(k) 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. The listed applicant is Baisheng Medical Co., Ltd.. The 510(k) number is K251235.

When did Electrosurgical Pads receive FDA 510(k) clearance?

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

Who is the listed applicant for Electrosurgical Pads?

The FDA 510(k) record lists Baisheng Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Electrosurgical Pads?

The FDA product code for Electrosurgical Pads is GEI.

Other records listing Baisheng Medical Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: GEI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.