K-number	K791776
Device name	ARRHYTHMIA II EDITOR
Applicant	Spacelabs, Inc.
Product code	DQK
Device class	Class II
Decision date	Oct 2, 1979
Decision	Substantially Equivalent
Regulation	870.1425

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View the full FDA submission: accessdata.fda.gov

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ARRHYTHMIA II EDITOR

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