K-number	K022219
Device name	EXOMIO, MODEL 1.1
Applicant	Medcom GmbH
Product code	KPQ
Device class	Class II
Decision date	Oct 7, 2002
Decision	Substantially Equivalent
Regulation	892.5840

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View the full FDA submission: accessdata.fda.gov

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EXOMIO, MODEL 1.1

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