K-number	K903505
Device name	BACT/ALERT (TM)
Applicant	Organon Teknika Corp.
Product code	MDB
Device class	Class I
Decision date	Mar 12, 1991
Decision	Substantially Equivalent
Regulation	866.2560

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View the full FDA submission: accessdata.fda.gov

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BACT/ALERT (TM)

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