K-number	K913594
Device name	DYNEX IIIB, MODEL 89002026
Applicant	Medtronic Vascular
Product code	GZJ
Device class	Class II
Decision date	Aug 23, 1991
Decision	Substantially Equivalent
Regulation	882.5890

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View the full FDA submission: accessdata.fda.gov

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DYNEX IIIB, MODEL 89002026

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