FDA 510(k) Application Details - K070446

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K070446
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	VALLEYLAB,A DIVISION OF TYCO HEALTHCARE GROUP LP 5920 LONGBOW DR. BOULDER, CO 80301 US Other 510(k) Applications for this Company
Contact	JULIE ROSS 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	02/15/2007
Decision Date	05/02/2007
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	N
Expedited Review