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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Radioimmunoassay, Thyroid-Stimulating Hormone
510(k) Number K221225
Device Name Access TSH (3rd IS) Assay, DxI 9000 Access Immunoassay Analyzer
Applicant
Beckman Coulter, Inc.
1000 Lake Hazeltine Drive
Chaska,  MN  55318
Applicant Contact Kuljeet Kaur
Correspondent
Beckman Coulter, Inc.
1000 Lake Hazeltine Drive
Chaska,  MN  55318
Correspondent Contact Kuljeet Kaur
Regulation Number862.1690
Classification Product Code
JLW  
Subsequent Product Code
JJE  
Date Received04/28/2022
Decision Date 11/10/2022
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Summary Summary
FDA Review Decision Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
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