K-number	K062769
Device name	PRESSUREWIRE CERTUS, MODELS 12006 AND 12306
Applicant	Radi Medical Systems AB
Product code	DXO
Device class	Class II
Decision date	Dec 4, 2006
Decision	Substantially Equivalent
Regulation	870.2870

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View the full FDA submission: accessdata.fda.gov

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PRESSUREWIRE CERTUS, MODELS 12006 AND 12306

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