K-number	K051258
Device name	KODAK DIRECTVIEW DR 7500 SYSTEM, MODEL 8791345
Applicant	Eastman Kodak Company
Product code	KPR
Device class	Class II
Decision date	Jun 1, 2005
Decision	Substantially Equivalent
Regulation	892.1680

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View the full FDA submission: accessdata.fda.gov

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KODAK DIRECTVIEW DR 7500 SYSTEM, MODEL 8791345

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