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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name radioimmunoassay, total thyroxine
510(k) Number K780854
Device Name IN VITRO NEONATAL T4
Applicant
CLINICAL ASSAYS, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
CLINICAL ASSAYS, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number862.1700
Classification Product Code
CDX  
Date Received05/22/1978
Decision Date 07/27/1978
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Microbiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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