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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Apparatus, Automated Blood Cell Diluting
510(k) Number K852373
Device Name AD150, AUTOMATED HEMATOLOGY DILUTOR
Applicant
Abbott Diagnostics
850 Maude Ave.
Mountain View,  CA  94043
Applicant Contact RUTH M BECKER
Correspondent
Abbott Diagnostics
850 Maude Ave.
Mountain View,  CA  94043
Correspondent Contact RUTH M BECKER
Regulation Number864.5240
Classification Product Code
GKH  
Date Received06/04/1985
Decision Date 07/05/1985
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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