K-number	K781641
Device name	SURGITEK DOUBLE J URETEROL STENT
Applicant	Medical Engineering Corp.
Product code	FAD
Device class	Class II
Decision date	Dec 7, 1978
Decision	Substantially Equivalent
Regulation	876.4620

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View the full FDA submission: accessdata.fda.gov

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SURGITEK DOUBLE J URETEROL STENT

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