FDA 510(k) Application Details - K070456

Device Classification Name	Catheter, Intravascular, Diagnostic   More FDA Info for this Device
510(K) Number	K070456
Device Name	Catheter, Intravascular, Diagnostic
Applicant	MICRUS ENDOVASCULAR CORPORATION 821 FOX LANE SAN JOSE, CA 95131 US Other 510(k) Applications for this Company
Contact	R. MICHAEL CROMPTON Other 510(k) Applications for this Contact
Regulation Number	870.1200   More FDA Info for this Regulation Number
Classification Product Code	DQO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/16/2007
Decision Date	05/24/2007
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