FDA 510(k) Application Details - K233525

Device Classification Name	Stimulator, Transcutaneous Electrical, Aesthetic Purposes   More FDA Info for this Device
510(K) Number	K233525
Device Name	Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Applicant	Micro Current Technology, Inc. 2244 1st Ave South Seattle, WA 98134 US Other 510(k) Applications for this Company
Contact	David Suzuki 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	11/01/2023
Decision Date	11/24/2023
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	Y
Expedited Review