FDA 510(k) Application Details - K070539

Device Classification Name	Electrocardiograph   More FDA Info for this Device
510(K) Number	K070539
Device Name	Electrocardiograph
Applicant	MORTARA INSTRUMENT, INC. 7865 NORTH 86TH ST. MILWAUKEE, WI 53224 US Other 510(k) Applications for this Company
Contact	LAURA M SPIEGELHOFF Other 510(k) Applications for this Contact
Regulation Number	870.2340   More FDA Info for this Regulation Number
Classification Product Code	DPS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/26/2007
Decision Date	03/15/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review