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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name test, qualitative and quantitative factor deficiency
510(k) Number K912468
Device Name LIATEST PROTEIN S KIT
Applicant
AMERICAN BIOPRODUCTS CO.
601 NORTH JEFFERSON RD.
PARSIPPANY,  NJ  07054
Applicant Contact LOC B LE
Correspondent
AMERICAN BIOPRODUCTS CO.
601 NORTH JEFFERSON RD.
PARSIPPANY,  NJ  07054
Correspondent Contact LOC B LE
Regulation Number864.7290
Classification Product Code
GGP  
Date Received06/04/1991
Decision Date 10/02/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Hematology
510k Review Panel Hematology
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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