FDA 510(k) Application Details - K243243

Device Classification Name	Electrode, Cutaneous   More FDA Info for this Device
510(K) Number	K243243
Device Name	Electrode, Cutaneous
Applicant	QuantalX Neuroscience, Ltd. 1 Hatachana st. Kfar Sava 4453001 IL Other 510(k) Applications for this Company
Contact	Hlila Fogel Other 510(k) Applications for this Contact
Regulation Number	882.1320   More FDA Info for this Regulation Number
Classification Product Code	GXY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/11/2024
Decision Date	02/06/2025
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