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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes
510(k) Number K781609
Device Name ALKALINE PHOSPHATASE IN SERUM
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 Number862.1050
Classification Product Code
CJE  
Date Received09/19/1978
Decision Date 10/24/1978
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Hematology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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