K-number	K113558
Device name	BD BACTEC Plus Aerobic/F Culture Vials (plastic)
Applicant	Becton, Dickinson and Company
Product code	MDB
Device class	Class I
Decision date	Mar 16, 2012
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 (plastic)

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