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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Acid, Uric, Acid Reduction Of Ferric Ion
510(k) Number K844075
Device Name URIC ACID REAGENT SET
Applicant
Livonia Diagnostics, Inc.
33041 W. Eight Mile Rd.
Livonia,  MI  48152
Applicant Contact WALTER H LAMBERT
Correspondent
Livonia Diagnostics, Inc.
33041 W. Eight Mile Rd.
Livonia,  MI  48152
Correspondent Contact WALTER H LAMBERT
Regulation Number862.1775
Classification Product Code
LFQ  
Date Received10/19/1984
Decision Date 10/30/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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