K-number	K790739
Device name	QUINTON MODEL 530X ECG DATA CART
Applicant	Quinton, Inc.
Product code	DPS
Device class	Class II
Decision date	Apr 26, 1979
Decision	Substantially Equivalent
Regulation	870.2340

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View the full FDA submission: accessdata.fda.gov

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QUINTON MODEL 530X ECG DATA CART

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