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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name counter, differential cell
510(k) Number K061667
Device Name CELL-DYN RUBY SYSTEM
Original Applicant
ABBOTT LABORATORIES
5440 patrick henry dr.
santa clara,  CA  95054
Original Contact michelle roeding
Regulation Number864.5220
Classification Product Code
GKZ  
Date Received06/14/2006
Decision Date 07/10/2006
Decision substantially equivalent (SESE)
Regulation Medical Specialty Hematology
510k Review Panel Hematology
summary summary
FDA Review Decision Summary
Type Special
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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