K-number	K960382
Device name	KODAK DIGITAL SCIENCE MEDICAL IMAGE MANAGER
Applicant	Eastman Kodak Company
Product code	LMD
Device class	Class I
Decision date	Apr 17, 1996
Decision	Substantially Equivalent
Regulation	892.2020

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View the full FDA submission: accessdata.fda.gov

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KODAK DIGITAL SCIENCE MEDICAL IMAGE MANAGER

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