K-number	K021829
Device name	MODIFICATION TO KODAK DIRECTVIEW CR 800/900 SYSTEM
Applicant	Eastman Kodak Company
Product code	MQB
Device class	Class II
Decision date	Jul 2, 2002
Decision	Substantially Equivalent
Regulation	892.1680

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO KODAK DIRECTVIEW CR 800/900 SYSTEM

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