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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name instrument, coagulation, automated
510(k) Number K160276
Device Name ACL TOP (ACL TOP 700, ACL TOP 700 CTS, ACL TOP 700 LAS, ACL TOP 500 CTS, ACL TOP 300 CTS)
Applicant
INSTRUMENTATION LABORATORY CO.
180 HARTWELL ROAD
BEDFORD,  MA  01730 -2441
Applicant Contact NIKITA MALLADI
Correspondent
INSTRUMENTATION LABORATORY CO.
180 HARTWELL ROAD
BEDFORD,  MA  01730 -2441
Correspondent Contact NIKITA MALLADI
Regulation Number864.5400
Classification Product Code
GKP  
Date Received02/02/2016
Decision Date 03/03/2016
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
Recalls CDRH Recalls
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