FDA 510(k) Application Details - K130847

Device Classification Name	System, Optical Position/Movement Recording   More FDA Info for this Device
510(K) Number	K130847
Device Name	System, Optical Position/Movement Recording
Applicant	JINTRONIX INC. 336 BRONTE ST SOUTH SUITE 224-225 MILTON, ONTARIO L9T 7W6 CA Other 510(k) Applications for this Company
Contact	NAVNEET SEKHON Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LXJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/26/2013
Decision Date	02/28/2014
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