K-number	K982263
Device name	MB/BACT BLOOD CULTURE BOTTLE
Applicant	Organon Teknika Corp.
Product code	MDB
Device class	Class I
Decision date	Aug 18, 1998
Decision	Substantially Equivalent
Regulation	866.2560

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View the full FDA submission: accessdata.fda.gov

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MB/BACT BLOOD CULTURE BOTTLE

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