K-number	K984532
Device name	CADPLAN HELIOS OPTION 6.0
Applicant	Varian Medical Systems, Inc.
Product code	MUJ
Device class	Class II
Decision date	Aug 9, 1999
Decision	Substantially Equivalent
Regulation	892.5050

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View the full FDA submission: accessdata.fda.gov

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CADPLAN HELIOS OPTION 6.0

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