FDA 510(k) Application Details - K041019

Device Classification Name	Apparatus, Cutting, Radiofrequency, Electrosurgical, Battery-Powered   More FDA Info for this Device
510(K) Number	K041019
Device Name	Apparatus, Cutting, Radiofrequency, Electrosurgical, Battery-Powered
Applicant	MEDISURG LTD. 100 WEST FORNANCE ST. THE FUGO BUILDING NORRISTOWN, PA 19401 US Other 510(k) Applications for this Company
Contact	RICHARD J FUGO Other 510(k) Applications for this Contact
Regulation Number	886.4100   More FDA Info for this Regulation Number
Classification Product Code	NCR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/20/2004
Decision Date	10/08/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OP - Ophthalmic
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review