K-number	K020689
Device name	SHERLOCK MYCOBACTERIA IDENTIFICATION SYSTEM
Applicant	Midi, Inc.
Product code	NJO
Device class	Class I
Decision date	Oct 31, 2002
Decision	Substantially Equivalent
Regulation	866.3370

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View the full FDA submission: accessdata.fda.gov

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SHERLOCK MYCOBACTERIA IDENTIFICATION SYSTEM

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