FDA 510(k) Application Details - K031979

Device Classification Name	Light, Surgical, Ceiling Mounted   More FDA Info for this Device
510(K) Number	K031979
Device Name	Light, Surgical, Ceiling Mounted
Applicant	CONMED INTEGRATED SYSTEMS (CMIS) 1815 NW 169TH PLACE SUITE 4020 BEAVERTON, OR 97006 US Other 510(k) Applications for this Company
Contact	C. JEFF LIPPS 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	06/26/2003
Decision Date	07/25/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review