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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Counter, Cell, Automated (Particle Counter)
510(k) Number K803218
Device Name CELL DYN 800 HEMATOLOGY ANALYZER
Applicant
ABBOTT DIAGNOSTICS
850 MAUDE AVE.
MOUNTAIN VIEW,  CA  94043
Correspondent
ABBOTT DIAGNOSTICS
850 MAUDE AVE.
MOUNTAIN VIEW,  CA  94043
Regulation Number864.5200
Classification Product Code
GKL  
Date Received12/18/1980
Decision Date 06/09/1981
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Hematology
510k Review Panel Hematology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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