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FDA 510(k) Application Details - K052224
Device Classification Name
Dna-Reagents, Neisseria
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510(K) Number
K052224
Device Name
Dna-Reagents, Neisseria
Applicant
BECTON, DICKINSON & CO.
7 LOVETON CIR.
SPARKS, MD 21152-0999 US
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Contact
KATHRYN BABKA POWERS
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Regulation Number
866.3390
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Classification Product Code
LSL
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More FDA Info for this Product Code
Date Received
08/16/2005
Decision Date
09/12/2005
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
MI - Microbiology
Review Advisory Committee
MI - Microbiology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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