K-number	K103028
Device name	EEVATM PETRI DISH
Applicant	Auxogyn, Inc.
Product code	MQK
Device class	Class II
Decision date	Aug 11, 2011
Decision	Substantially Equivalent
Regulation	884.6160

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Source

View the full FDA submission: accessdata.fda.gov

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EEVATM PETRI DISH

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