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FDA 510(k) Application Details - K070691
Device Classification Name
Culture Media, Selective And Differential
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510(K) Number
K070691
Device Name
Culture Media, Selective And Differential
Applicant
BECTON, DICKINSON & CO.
7 LOVETON CIR.
SPARKS, MD 21152-0999 US
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Contact
DENNIS R MERTZ
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Regulation Number
866.2360
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Classification Product Code
JSI
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More FDA Info for this Product Code
Date Received
03/13/2007
Decision Date
11/20/2007
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
MI - Microbiology
Review Advisory Committee
MI - Microbiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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