K-number	K983928
Device name	KODAK HOME HEALTH MONITORING SYSTEM
Applicant	Eastman Kodak Company
Product code	MWI
Device class	Class II
Decision date	Feb 11, 2000
Decision	Substantially Equivalent
Regulation	870.2300

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View the full FDA submission: accessdata.fda.gov

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KODAK HOME HEALTH MONITORING SYSTEM

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