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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name urease and glutamic dehydrogenase, urea nitrogen
510(k) Number K982236
Device Name SIGMA DIAGNOSTICS INFINITY BUN REAGENT KIT
Applicant
SIGMA DIAGNOSTICS, INC.
545 SOUTH EWING AVE.
ST.LOUIS,  MO  63103
Applicant Contact WILLIAM R GILBERT
Correspondent
SIGMA DIAGNOSTICS, INC.
545 SOUTH EWING AVE.
ST.LOUIS,  MO  63103
Correspondent Contact WILLIAM R GILBERT
Regulation Number862.1770
Classification Product Code
CDQ  
Date Received06/25/1998
Decision Date 08/05/1998
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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