K-number	K820356
Device name	MULTICOR (GAMMA) 402 CARDIAC PACER
Applicant	Cordis Corp.
Product code	DXY
Device class	Class III
Decision date	Mar 18, 1982
Decision	Substantially Equivalent
Regulation	870.3610

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View the full FDA submission: accessdata.fda.gov

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MULTICOR (GAMMA) 402 CARDIAC PACER

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