K-number	K952430
Device name	FINESSE GUIDEWIRE CORONARY
Applicant	Flexmedics
Product code	DQX
Device class	Class II
Decision date	Aug 18, 1995
Decision	Substantially Equivalent
Regulation	870.1330

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Source

View the full FDA submission: accessdata.fda.gov

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FINESSE GUIDEWIRE CORONARY

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