K-number	K810734
Device name	MODELS 8420 THRU 8423 PACEMAKER GENER
Applicant	Medtronic Vascular
Product code	DXY
Device class	Class III
Decision date	May 15, 1981
Decision	Substantially Equivalent
Regulation	870.3610

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View the full FDA submission: accessdata.fda.gov

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MODELS 8420 THRU 8423 PACEMAKER GENER

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