FDA 510(k) Application Details - K061173

Device Classification Name	More FDA Info for this Device
510(K) Number	K061173
Device Name	CPIVISION DIGITAL IMAGING SYSTEM
Applicant	COMMUNICATIONS & POWER INDUSTRIES CANADA, INC. 45 RIVER DRIVE GEORGETOWN,ONTARIO L7G 2J4 CA Other 510(k) Applications for this Company
Contact	NORM MORIKAWA Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OWB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/27/2006
Decision Date	06/09/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review