FDA 510(k) Application Details - K014201

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K014201
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	AARON MEDICAL INDUSTRIES 7100 30TH AVE. NORTH ST. PETERSBURG, FL 33710-2902 US Other 510(k) Applications for this Company
Contact	RICHARD A KOZLOFF 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	12/21/2001
Decision Date	02/25/2002
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