K-number	K232870
Device name	TrueBeam, TrueBeam STx, EDGE and VitalBeam (4.1)
Applicant	Varian Medical Systems, Inc.
Product code	IYE
Device class	Class II
Decision date	Dec 21, 2023
Decision	Substantially Equivalent
Regulation	892.5050

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View the full FDA submission: accessdata.fda.gov

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TrueBeam, TrueBeam STx, EDGE and VitalBeam (4.1)

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