K-number	K032129
Device name	RADIUS 018 COUGAR WIRE
Applicant	Radius Medical Technologies, Inc.
Product code	DQX
Device class	Class II
Decision date	Jul 17, 2003
Decision	Substantially Equivalent
Regulation	870.1330

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View the full FDA submission: accessdata.fda.gov

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RADIUS 018 COUGAR WIRE

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