K-number	K983506
Device name	PRESSUREWIRE SENSOR, MODEL #12001
Applicant	Radi Medical Systems AB
Product code	DQX
Device class	Class II
Decision date	Feb 3, 1999
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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PRESSUREWIRE SENSOR, MODEL #12001

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