FDA 510(k) Application Details - K081939

Device Classification Name	Powered Laser Surgical Instrument   More FDA Info for this Device
510(K) Number	K081939
Device Name	Powered Laser Surgical Instrument
Applicant	OMNIGUIDE, INC. ONE KENDALL SQUARE, BLDG 100 3RD FLOOR CAMBRIDGE, MA 02139 US Other 510(k) Applications for this Company
Contact	DOUGLAS W WOODRUFF Other 510(k) Applications for this Contact
Regulation Number	878.4810   More FDA Info for this Regulation Number
Classification Product Code	GEX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/08/2008
Decision Date	08/12/2008
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