FDA 510(k) Application Details - K142254

Device Classification Name	Wire, Guide, Catheter   More FDA Info for this Device
510(K) Number	K142254
Device Name	Wire, Guide, Catheter
Applicant	St. Jude Medical 15900 Valley View Court Sylmar, CA 91342 US Other 510(k) Applications for this Company
Contact	Geena George Other 510(k) Applications for this Contact
Regulation Number	870.1330   More FDA Info for this Regulation Number
Classification Product Code	DQX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/14/2014
Decision Date	11/13/2014
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