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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 K162414
Device Name UniCel DxH SlideMaker Stainer Coulter Cellular Analysis System
Applicant
Beckman Coulter, Inc.
11800 SW 147th Ave.
Miami,  FL  33196
Applicant Contact NANCY NADLER
Correspondent
Beckman Coulter, Inc.
11800 SW 147th Ave.
Miami,  FL  33196
Correspondent Contact NANCY NADLER
Regulation Number864.5220
Classification Product Code
GKZ  
Date Received08/29/2016
Decision Date 11/29/2016
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
Predetermined Change
Control Plan Authorized		 No
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