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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 K862210
Device Name UREA NITROGEN (GLDH) REAGENT SET (UV)
Applicant
Sterling Diagnostics, Inc.
34210 Dequindre Rd.
Sterling Heights,  MI  48077
Applicant Contact DAVID L CALLENDER
Correspondent
Sterling Diagnostics, Inc.
34210 Dequindre Rd.
Sterling Heights,  MI  48077
Correspondent Contact DAVID L CALLENDER
Regulation Number862.1770
Classification Product Code
CDQ  
Date Received06/10/1986
Decision Date 07/01/1986
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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