FDA 510(k) Application Details - K131816

Device Classification Name	Display, Cathode-Ray Tube, Medical   More FDA Info for this Device
510(K) Number	K131816
Device Name	Display, Cathode-Ray Tube, Medical
Applicant	SORIN GROUP DEUTSCHLAND GMBH LINDBERGH STRASSE 25 MUNCHEN 80939 DE Other 510(k) Applications for this Company
Contact	RENATE GOEBERT Other 510(k) Applications for this Contact
Regulation Number	870.2450   More FDA Info for this Regulation Number
Classification Product Code	DXJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/20/2013
Decision Date	07/23/2013
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	Y
Expedited Review