K-number	K841611
Device name	QUINTON 901 & 900 HOLTER SCANNER
Applicant	Quinton, Inc.
Product code	DPS
Device class	Class II
Decision date	Aug 2, 1984
Decision	Substantially Equivalent
Regulation	870.2340

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View the full FDA submission: accessdata.fda.gov

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QUINTON 901 & 900 HOLTER SCANNER

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