K-number	K910691
Device name	NORTEC URETERAL STENT
Applicant	North American Sterilization & Packaging Co.
Product code	FAD
Device class	Class II
Decision date	Aug 15, 1991
Decision	Substantially Equivalent
Regulation	876.4620

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View the full FDA submission: accessdata.fda.gov

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NORTEC URETERAL STENT

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