FDA 510(k) Application Details - K250360

Device Classification Name	Stimulator, Nerve, Transcutaneous, Over-The-Counter   More FDA Info for this Device
510(K) Number	K250360
Device Name	Stimulator, Nerve, Transcutaneous, Over-The-Counter
Applicant	Shenzhen Jiantuo Electronics Co., Ltd. 608, Block A, Zhuoyue Yulong Haoxuan, Xinyang Community Shajing Street, Bao'an District Shenzhen 518104 CN Other 510(k) Applications for this Company
Contact	Jin Liang Zou Other 510(k) Applications for this Contact
Regulation Number	882.5890   More FDA Info for this Regulation Number
Classification Product Code	NUH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/10/2025
Decision Date	05/11/2025
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review