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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, phosphotungstate reduction
510(k) Number K770459
Device Name URIC ACID PROCEDURE, TEKPOINT DIRECT
Applicant
ICN PHARMACEUTICALS, INC.
13 MOUNTAINVIEW AVE.
ORANGEBURG,  NY  10962
Correspondent
ICN PHARMACEUTICALS, INC.
13 MOUNTAINVIEW AVE.
ORANGEBURG,  NY  10962
Regulation Number862.1775
Classification Product Code
CDH  
Date Received03/08/1977
Decision Date 04/29/1977
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
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