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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name system, test, thyroid autoantibody
510(k) Number K051890
Device Name ROCHE DIAGNOSTICS COBAS ELECSYS ANTI-TPO
Applicant
ROCHE DIAGNOSTICS CORP.
9115 HAGUE RD.
INDIANAPOLIS,  IN  46250
Applicant Contact KAY A TAYLOR
Correspondent
ROCHE DIAGNOSTICS CORP.
9115 HAGUE RD.
INDIANAPOLIS,  IN  46250
Correspondent Contact KAY A TAYLOR
Regulation Number866.5870
Classification Product Code
JZO  
Date Received07/12/2005
Decision Date 08/04/2005
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Immunology
510k Review Panel Immunology
Summary Summary
FDA Review Decision Summary
Type Special
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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