K-number	K905289
Device name	SURGITEK(R) LUBRI-FLEX(TM) URETERAL STENT
Applicant	Medical Engineering Corp.
Product code	FAD
Device class	Class II
Decision date	Mar 13, 1991
Decision	Substantially Equivalent
Regulation	876.4620

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View the full FDA submission: accessdata.fda.gov

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SURGITEK(R) LUBRI-FLEX(TM) URETERAL STENT

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