FDA 510(k) Application Details - K230459

Device Classification Name	Stimulator, Transcutaneous Electrical, Aesthetic Purposes   More FDA Info for this Device
510(K) Number	K230459
Device Name	Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Applicant	21 Equipment S.R.L. Piazza Bodoni 3 Torino 10123 IT Other 510(k) Applications for this Company
Contact	Dolores Moretto Other 510(k) Applications for this Contact
Regulation Number	882.5890   More FDA Info for this Regulation Number
Classification Product Code	NFO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/21/2023
Decision Date	10/19/2023
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