K-number	K083572
Device name	BD BACTEC Plus Aerobic/F Culture Vials
Applicant	Becton, Dickinson & CO
Product code	MDB
Device class	Class I
Decision date	Dec 24, 2008
Decision	Substantially Equivalent
Regulation	866.2560

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Source

View the full FDA submission: accessdata.fda.gov

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BD BACTEC Plus Aerobic/F Culture Vials

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