K-number	K030745
Device name	GAMMAMED 212 AND 232 SOURCE ASSEMBLY
Applicant	Varian Medical Systems
Product code	KXK
Device class	Class II
Decision date	Mar 12, 2003
Decision	Substantially Equivalent
Regulation	892.5730

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Source

View the full FDA submission: accessdata.fda.gov

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GAMMAMED 212 AND 232 SOURCE ASSEMBLY

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