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FDA 510(k) Application Details - K962671
Device Classification Name
Plasma, Coagulation Factor Deficient
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510(K) Number
K962671
Device Name
Plasma, Coagulation Factor Deficient
Applicant
AMERICAN BIOPRODUCTS CO.
5 CENTURY DR.
PARSIPPANY, NJ 07054 US
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Contact
ANDREW LOC B. LE
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Regulation Number
864.7290
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Classification Product Code
GJT
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More FDA Info for this Product Code
Date Received
07/09/1996
Decision Date
09/13/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HE - Hematology
Review Advisory Committee
HE - Hematology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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