FDA 510(k) Application Details - K133534

Device Classification Name	Computer, Diagnostic, Programmable   More FDA Info for this Device
510(K) Number	K133534
Device Name	Computer, Diagnostic, Programmable
Applicant	MCKESSON ISRAEL LTD. 5995 WINDWARD PARKWAY ALPHARETTA, GA 30005 US Other 510(k) Applications for this Company
Contact	PAUL SUMNER Other 510(k) Applications for this Contact
Regulation Number	870.1425   More FDA Info for this Regulation Number
Classification Product Code	DQK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/18/2013
Decision Date	04/18/2014
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