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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Assay, Glycosylated Hemoglobin
510(k) Number K802432
Device Name GLYCO-TROL HUMAN GLYCOSYLATED HOM. CONT.
Applicant
Clin Tech Diagnostics Corp.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Clin Tech Diagnostics Corp.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number864.7470
Classification Product Code
LCP  
Date Received10/06/1980
Decision Date 12/01/1980
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Hematology
510k Review Panel Hematology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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