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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 K790800
Device Name CENTRIA T4 RIA TEST SET
Applicant
VENTREX LABORATORIES, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
VENTREX LABORATORIES, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number862.1700
Classification Product Code
CDX  
Date Received04/24/1979
Decision Date 06/15/1979
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Toxicology
Type Traditional
Reviewed by Third Party No
Combination Product No
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