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FDA 510(k) Application Details - K152870
Device Classification Name
More FDA Info for this Device
510(K) Number
K152870
Device Name
BD Veritor System for the Rapid Detection of Flu A + B CLIA waived kit
Applicant
BECTON DICKINSON AND CO.
10865 ROAD TO THE CURE, SUITE 200
SAN DIEGO, CA 92121 US
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Contact
GREGORY P. PAYNE
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Regulation Number
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Classification Product Code
PSZ
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Date Received
09/30/2015
Decision Date
10/27/2015
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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