FDA 510(k) Application Details - K150959

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K150959
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	SUTTER MEDIZINTECHNIK GMBH TULLASTRASSE 87 FREIBURG 79108 DE Other 510(k) Applications for this Company
Contact	BERT SUTTER 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	04/10/2015
Decision Date	09/10/2015
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