K-number	K001006
Device name	THERATRON 780C/1000 WITH COMPUTERIZED CONSOLE UPGRADE
Applicant	Mds Nordion
Product code	IWB
Device class	Class II
Decision date	Apr 27, 2000
Decision	Substantially Equivalent
Regulation	892.5750

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View the full FDA submission: accessdata.fda.gov

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THERATRON 780C/1000 WITH COMPUTERIZED CONSOLE UPGRADE

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