K-number	K771992
Device name	L-501 CARDIAC PACEMAKER
Applicant	Coratomic, Inc.
Product code	DXY
Device class	Class III
Decision date	Nov 2, 1977
Decision	Substantially Equivalent
Regulation	870.3610

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View the full FDA submission: accessdata.fda.gov

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L-501 CARDIAC PACEMAKER

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