K-number	K880738
Device name	MODEL 2331T PATIENT PROGRAMMER
Applicant	Medtronic Vascular
Product code	KRG
Device class	Class III
Decision date	Nov 17, 1988
Decision	Substantially Equivalent
Regulation	870.3700

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View the full FDA submission: accessdata.fda.gov

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MODEL 2331T PATIENT PROGRAMMER

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