FDA 510(k) Application Details - K992760

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K992760
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	SELECT MEDIZINTECHNIK HERMANN SUTTER GMBH 9070 BLUFFVIEW TRACE ROSWELL, GA 30076 US Other 510(k) Applications for this Company
Contact	ANITA THIBEAULT 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	08/17/1999
Decision Date	10/25/1999
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