FDA 510(k) Application Details - K133273

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K133273
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	LIGER MEDICAL, LLC 825 N 300 WEST #NE127 SALT LAKE CITY, UT 84103 US Other 510(k) Applications for this Company
Contact	STEVE SMITH 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	10/24/2013
Decision Date	02/12/2014
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