K-number	K772202
Device name	PULSE GENERATOR, A-V SEQ.
Applicant	Medtronic Vascular
Product code	DXY
Device class	Class III
Decision date	Dec 20, 1977
Decision	Substantially Equivalent
Regulation	870.3610

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View the full FDA submission: accessdata.fda.gov

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PULSE GENERATOR, A-V SEQ.

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