FDA 510(k) Application Details - K120834

Device Classification Name	System, Catheter Control, Steerable   More FDA Info for this Device
510(K) Number	K120834
Device Name	System, Catheter Control, Steerable
Applicant	CORINDUS INC. 5523 RESEARCH PARK DRIVE SUITE 110 BALTIMORE, MD 21228 US Other 510(k) Applications for this Company
Contact	MONA ADVANI Other 510(k) Applications for this Contact
Regulation Number	870.1290   More FDA Info for this Regulation Number
Classification Product Code	DXX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/19/2012
Decision Date	07/19/2012
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