FDA 510(k) Application Details - K133865

Device Classification Name	Wire, Guide, Catheter   More FDA Info for this Device
510(K) Number	K133865
Device Name	Wire, Guide, Catheter
Applicant	ASAHI INTECC CO., LTD. 5523 RESEARCH PARK DRIVE, SUITE 205 BALTIMORE, MD 21228 US Other 510(k) Applications for this Company
Contact	CANDACE CEDERMAN 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	12/19/2013
Decision Date	03/18/2014
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