FDA 510(k) Application Details - K033997

Device Classification Name	Catheter, Peripheral, Atherectomy   More FDA Info for this Device
510(K) Number	K033997
Device Name	Catheter, Peripheral, Atherectomy
Applicant	BACCHUS VASCULAR, INC. 3110 CORONADO DR. SANTA CLARA, CA 95054 US Other 510(k) Applications for this Company
Contact	LISA CAPARRA Other 510(k) Applications for this Contact
Regulation Number	870.4875   More FDA Info for this Regulation Number
Classification Product Code	MCW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/24/2003
Decision Date	02/04/2004
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