K-number	K821173
Device name	EVENTMASTER 3 HOLTER EVENT SCANNER
Applicant	Instruments For Cardiac Research
Product code	DSF
Device class	Class I
Decision date	May 18, 1982
Decision	Substantially Equivalent
Regulation	870.2810

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View the full FDA submission: accessdata.fda.gov

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EVENTMASTER 3 HOLTER EVENT SCANNER

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