K-number	K083264
Device name	RAYAUTOPLAN 1.0
Applicant	Raysearch Laboratories AB
Product code	MUJ
Device class	Class II
Decision date	Jan 22, 2009
Decision	Substantially Equivalent
Regulation	892.5050

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Source

View the full FDA submission: accessdata.fda.gov

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RAYAUTOPLAN 1.0

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