K-number	K052323
Device name	VERSATREK MYCO PZA KIT
Applicant	Trek Diagnostic Systems, Inc.
Product code	MJA
Device class	Class II
Decision date	Jan 19, 2006
Decision	Substantially Equivalent
Regulation	866.1640

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View the full FDA submission: accessdata.fda.gov

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VERSATREK MYCO PZA KIT

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