FDA 510(k) Application Details - K003471

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K003471
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	HUTTINGER MEDIZINTECHNIK GMBH & CO KG AM GANSACKER 1B UMKIRCH 79224 DE Other 510(k) Applications for this Company
Contact	BERNHARD HUG 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	11/08/2000
Decision Date	11/20/2000
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	Y
Expedited Review