FDA 510(k) Application Details - K951130

Device Classification Name	System, Ecg Analysis   More FDA Info for this Device
510(K) Number	K951130
Device Name	System, Ecg Analysis
Applicant	MARQUETTE ELECTRONICS, INC. 8200 WEST TOWER AVE. MILWAUKEE, WI 53223 US Other 510(k) Applications for this Company
Contact	KRISTIN PABST Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LOS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/13/1995
Decision Date	04/04/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review