FDA 510(k) Application Details - K992090

Device Classification Name	Light, Surgical, Ceiling Mounted   More FDA Info for this Device
510(K) Number	K992090
Device Name	Light, Surgical, Ceiling Mounted
Applicant	SKYTRON, DIV. THE KMW GROUP, INC. 5000 36TH ST., S.E. GRAND RAPIDS, MI 49512 US Other 510(k) Applications for this Company
Contact	KARI OGREEN 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	06/21/1999
Decision Date	09/08/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review