FDA 510(k) Application Details - K070166

Device Classification Name	Introducer, Catheter   More FDA Info for this Device
510(K) Number	K070166
Device Name	Introducer, Catheter
Applicant	ST. JUDE MEDICAL 6550 WEDGWOOD RD. NORTH SUITE 150 MAPLE GROVE, MN 55311 US Other 510(k) Applications for this Company
Contact	JEFF STURM Other 510(k) Applications for this Contact
Regulation Number	870.1340   More FDA Info for this Regulation Number
Classification Product Code	DYB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/18/2007
Decision Date	04/06/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review