K-number	K802357
Device name	TELEMETRY PACEMAKER MONITOR
Applicant	Intermedics, Inc.
Product code	DRG
Device class	Class II
Decision date	Feb 12, 1981
Decision	Substantially Equivalent
Regulation	870.2910

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View the full FDA submission: accessdata.fda.gov

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TELEMETRY PACEMAKER MONITOR

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