FDA 510(k) Application Details - K982425

Device Classification Name	System, Optical Position/Movement Recording   More FDA Info for this Device
510(K) Number	K982425
Device Name	System, Optical Position/Movement Recording
Applicant	PINSCO INC. DBA B & L ENGINEERING 3002 DOW AVENUE, SUITE 416 TUSTIN, CA 92780 US Other 510(k) Applications for this Company
Contact	LEE A BARNES 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	07/13/1998
Decision Date	10/07/1998
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