K-number	K090824
Device name	BD PROBETEC CHLAMYDIA TRACHOMATIS (CT) QX AMPLIFIED DNA ASSAY
Applicant	Becton, Dickinson & CO
Product code	MKZ
Device class	Class I
Decision date	Jun 2, 2009
Decision	Substantially Equivalent
Regulation	866.3120

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View the full FDA submission: accessdata.fda.gov

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BD PROBETEC CHLAMYDIA TRACHOMATIS (CT) QX AMPLIFIED DNA ASSAY

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