K-number	K822319
Device name	RE1000 HEART RATE MONITOR
Applicant	Electronic Monitors, Inc.
Product code	DRT
Device class	Class II
Decision date	Sep 14, 1982
Decision	Substantially Equivalent
Regulation	870.2300

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View the full FDA submission: accessdata.fda.gov

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RE1000 HEART RATE MONITOR

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