FDA 510(k) Application Details - K241601

Device Classification Name	Stimulator, Muscle, Powered, For Muscle Conditioning   More FDA Info for this Device
510(K) Number	K241601
Device Name	Stimulator, Muscle, Powered, For Muscle Conditioning
Applicant	CPMT LASER (Canadian Pioneer Medical Technology Corporation) 460 Garyray Drive, North York Toronto M9L1P8 CA Other 510(k) Applications for this Company
Contact	Rashid Reza Mir Sayah Other 510(k) Applications for this Contact
Regulation Number	890.5850   More FDA Info for this Regulation Number
Classification Product Code	NGX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/04/2024
Decision Date	02/25/2025
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review