FDA 510(k) Application Details - K052022

Device Classification Name	Wire, Guide, Catheter   More FDA Info for this Device
510(K) Number	K052022
Device Name	Wire, Guide, Catheter
Applicant	ASAHI INTECC CO., LTD. 1301 DOVE STREET, SUITE #350 NEWPORT BEACH, CA 92660 US Other 510(k) Applications for this Company
Contact	YOSHI TERAI 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	07/26/2005
Decision Date	08/25/2005
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