K-number	K063482
Device name	CROSSPLAN / ACCUSOFT-XL V.4.04
Applicant	Direx Systems Corp.
Product code	MUJ
Device class	Class II
Decision date	Dec 14, 2006
Decision	Substantially Equivalent
Regulation	892.5050

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View the full FDA submission: accessdata.fda.gov

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CROSSPLAN / ACCUSOFT-XL V.4.04

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