FDA 510(k) Application Details - K151877

Device Classification Name	Dilator, Vessel, For Percutaneous Catheterization   More FDA Info for this Device
510(K) Number	K151877
Device Name	Dilator, Vessel, For Percutaneous Catheterization
Applicant	ARSTASIS, INC. 6500 KAISER DRIVE SUITE 120 FREMONT, CA 94555 US Other 510(k) Applications for this Company
Contact	Debra Cogan Other 510(k) Applications for this Contact
Regulation Number	870.1310   More FDA Info for this Regulation Number
Classification Product Code	DRE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/09/2015
Decision Date	08/07/2015
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