FDA 510(k) Application Details - K240292

Device Classification Name	Stimulator, Nerve, Transcutaneous, Over-The-Counter   More FDA Info for this Device
510(K) Number	K240292
Device Name	Stimulator, Nerve, Transcutaneous, Over-The-Counter
Applicant	Hong Kong Etech Groups Limited Rm 747,7/F Star Hse 3 Salisbury Rd Tst Hong Kong 999077 CN Other 510(k) Applications for this Company
Contact	Haixin Chen 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	02/01/2024
Decision Date	03/25/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review