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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name analyzer, chemistry (photometric, discrete), for clinical use
510(k) Number K834521
Device Name DISCRETE CLINICAL ANALYZER
Applicant
E.I. DUPONT DE NEMOURS & CO., INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
E.I. DUPONT DE NEMOURS & CO., INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number862.2160
Classification Product Code
JJE  
Date Received12/21/1983
Decision Date 02/27/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
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