K-number	K082061
Device name	INQUIRY H-CURVE TV STEERABLE DIAGNOSTIC CATHETER
Applicant	Irvine Biomedical, Inc.
Product code	DRF
Device class	Class II
Decision date	Aug 19, 2008
Decision	Substantially Equivalent
Regulation	870.1220

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View the full FDA submission: accessdata.fda.gov

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INQUIRY H-CURVE TV STEERABLE DIAGNOSTIC CATHETER

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