FDA 510(k) Application Details - K151446

Device Classification Name	System, Optical Position/Movement Recording   More FDA Info for this Device
510(K) Number	K151446
Device Name	System, Optical Position/Movement Recording
Applicant	Recovr,Inc Post Office Box 772 Clemson, SC 29633 US Other 510(k) Applications for this Company
Contact	Austen Hayes 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	05/29/2015
Decision Date	09/18/2015
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