FDA 510(k) Application Details - K002877

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K002877
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	DUFNER INSTRUMENTE GMBH AMSTEL 320-I AMSTERDAM 1017AP NL Other 510(k) Applications for this Company
Contact	DAGMAR MASER 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	09/15/2000
Decision Date	02/05/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review