K-number	K060302
Device name	INSCOPE PRECISION BALLOON DILATOR - WIRE GUIDED
Applicant	Cordis Europa, N.V.
Product code	KNQ
Device class	Class II
Decision date	Apr 11, 2006
Decision	Substantially Equivalent
Regulation	876.5365

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View the full FDA submission: accessdata.fda.gov

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INSCOPE PRECISION BALLOON DILATOR - WIRE GUIDED

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