FDA 510(k) Application Details - K061173

Device Classification Name

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510(K) Number K061173
Device Name CPIVISION DIGITAL IMAGING SYSTEM
Applicant COMMUNICATIONS & POWER INDUSTRIES CANADA, INC.
45 RIVER DRIVE
GEORGETOWN,ONTARIO L7G 2J4 CA
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Contact NORM MORIKAWA
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Regulation Number

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Classification Product Code OWB
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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



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