K-number	K150246
Device name	Medtronic Model 5392 External Pulse Generator (EPG)
Applicant	Medtronic, Inc.
Product code	DTE
Device class	Class II
Decision date	Feb 18, 2015
Decision	Substantially Equivalent
Regulation	870.3600

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View the full FDA submission: accessdata.fda.gov

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Medtronic Model 5392 External Pulse Generator (EPG)

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