FDA 510(k) Application Details - K123310

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K123310
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	UTAH MEDICAL PRODUCTS, INC. 7043 South 300 West Midvale, UT 84047 US Other 510(k) Applications for this Company
Contact	BEN SHIRLEY 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	10/25/2012
Decision Date	01/23/2013
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	Y
Expedited Review