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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name System, Test, Automated Blood Grouping And Antibody
510(k) Number K771098
Device Name BLOOD GROUPING SYS., BG-9
Applicant
TECHNICON INSTRUMENTS CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
TECHNICON INSTRUMENTS CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number864.9175
Classification Product Code
KSZ  
Date Received06/20/1977
Decision Date 08/04/1977
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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