510(k) K250841

Device
Electrotherapy Electrodes
Applicant
Baisheng Medical Co., Ltd.
510(k) number
K250841
Product code
GXY
Decision
Substantially Equivalent (SESE)
Decision date
2025-08-13
Date received
2025-03-20
Regulation
882.1320
Classification name
Electrode, Cutaneous
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Xi Chen
Address
#11, Fusheng Rd.,Xinhui District Jiangmen Guangdong CN 529100 529100

FDA Registration Numbers

Source Documents

510(k) summary PDF

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