FDA 510(k) Application Details - K041981

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K041981
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	GUIDANT CORPORATION 3200 LAKESIDE DR. SANTA CLARA, CA 95054 US Other 510(k) Applications for this Company
Contact	M. LAURIE WONG Other 510(k) Applications for this Contact
Regulation Number	878.4400   More FDA Info for this Regulation Number
Classification Product Code	GEI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/23/2004
Decision Date	08/20/2004
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