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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 K850933
Device Name URIC ACID
Applicant
Dilab, Inc.
7003 NW 50th St.
Miami,  FL  33166
Applicant Contact RAFAEL A QUEVEDO
Correspondent
Dilab, Inc.
7003 NW 50th St.
Miami,  FL  33166
Correspondent Contact RAFAEL A QUEVEDO
Regulation Number862.1775
Classification Product Code
CDH  
Date Received03/07/1985
Decision Date 06/25/1985
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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