FDA 510(k) Application Details - K060802

Device Classification Name	Light, Surgical, Ceiling Mounted   More FDA Info for this Device
510(K) Number	K060802
Device Name	Light, Surgical, Ceiling Mounted
Applicant	STRYKER COMMUNICATIONS CORP. 1410 LAKESIDE PKWY., #100 FLOWER MOUND, TX 75028 US Other 510(k) Applications for this Company
Contact	LOUIS-PIERRE MARCOUX Other 510(k) Applications for this Contact
Regulation Number	878.4580   More FDA Info for this Regulation Number
Classification Product Code	FSY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/24/2006
Decision Date	04/07/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	Y
Expedited Review