K-number	K091370
Device name	RADIA STEERABLE DIAGNOSTIC CATHETER
Applicant	C.R. Bard, Inc.
Product code	DRF
Device class	Class II
Decision date	Jun 5, 2009
Decision	Substantially Equivalent
Regulation	870.1220

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View the full FDA submission: accessdata.fda.gov

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RADIA STEERABLE DIAGNOSTIC CATHETER

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