K-number	K072680
Device name	DRYSTAR AXYS, MODEL EYZ4E
Applicant	Agfa Healthcare Corporation
Product code	LMC
Device class	Class II
Decision date	Oct 25, 2007
Decision	Substantially Equivalent
Regulation	892.2040

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View the full FDA submission: accessdata.fda.gov

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DRYSTAR AXYS, MODEL EYZ4E

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