FDA 510(k) Application Details - K000496

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K000496
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	EVEREST MEDICAL CORP. 13755 FIRST AVENUE, NORTH, SUITE 500 MINNEAPOLIS, MN 55441-5444 US Other 510(k) Applications for this Company
Contact	FREDERICK G MADES 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	02/15/2000
Decision Date	04/24/2000
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