FDA 510(k) Application Details - K130669

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K130669
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	OLSEN MEDICAL 1927 N. ARTHUR DR. COLUMBIA CITY, IN 46725 US Other 510(k) Applications for this Company
Contact	DALENE BINKLEY 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	03/12/2013
Decision Date	12/06/2013
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