FDA 510(k) Application Details - K081940

Device Classification Name	Dilator, Vessel, For Percutaneous Catheterization   More FDA Info for this Device
510(K) Number	K081940
Device Name	Dilator, Vessel, For Percutaneous Catheterization
Applicant	AVALON LABORATORIES, LLC 2610 E. HOMESTEAD PLACE RANCHO DOMINGUEZ, CA 90220 US Other 510(k) Applications for this Company
Contact	LEE WIRTH 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	07/08/2008
Decision Date	11/18/2008
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