FDA 510(k) Application Details - K141153

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K141153
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	COVIDIEN 5920 LONGBOW DR. BOULDER, CO 80301 US Other 510(k) Applications for this Company
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	05/05/2014
Decision Date	08/14/2014
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