K-number	K102583
Device name	MUCHECK, VERSION 9.0
Applicant	Oncology Data Systems, Inc.
Product code	IYE
Device class	Class II
Decision date	Nov 2, 2010
Decision	Substantially Equivalent
Regulation	892.5050

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Source

View the full FDA submission: accessdata.fda.gov

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MUCHECK, VERSION 9.0

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