K-number	K761201
Device name	ECHO-CARDIOTRACE, AUTOMATIC
Applicant	Metrix Co.
Product code	HGM
Device class	Class II
Decision date	Jan 12, 1977
Decision	Substantially Equivalent
Regulation	884.2740

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View the full FDA submission: accessdata.fda.gov

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ECHO-CARDIOTRACE, AUTOMATIC

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