K-number	K885058
Device name	CARDIOCAP(TM) DR-104 REPORTER
Applicant	Datex Division Instrumentarium Corp.
Product code	DSF
Device class	Class I
Decision date	Jul 14, 1989
Decision	Substantially Equivalent
Regulation	870.2810

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View the full FDA submission: accessdata.fda.gov

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CARDIOCAP(TM) DR-104 REPORTER

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