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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Mixture, Hematology Quality Control
510(k) Number K792055
Device Name FISHER DIAGNOSTICS HEMATOLOGY CONTROLS
Applicant
Fisher Scientific Co., LLC
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Fisher Scientific Co., LLC
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number864.8625
Classification Product Code
JPK  
Date Received10/15/1979
Decision Date 11/05/1979
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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