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FDA 510(k) Applications for Medical Device Product Code "JSI"
(Culture Media, Selective And Differential)
FDA 510(k) Number
Applicant
Device Name
Decision Date
K070691
BECTON, DICKINSON & CO.
BBL CHROMAGAR 0157
11/20/2007
K974428
NOVAMED LTD.
DIPSTREAK
07/30/1998
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