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FDA 510(k) Application Details - K955561
Device Classification Name
Radioassay, Vitamin B12
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510(K) Number
K955561
Device Name
Radioassay, Vitamin B12
Applicant
AMERICAN LABORATORY PRODUCTS CO., LTD.
P.O. BOX 451
WINDHAM, NH 03087 US
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Contact
RICHARD E CONLEY
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Regulation Number
862.1810
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Classification Product Code
CDD
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More FDA Info for this Product Code
Date Received
12/06/1995
Decision Date
05/23/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CH - Clinical Chemistry
Review Advisory Committee
CH - Clinical Chemistry
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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