K-number	K021906
Device name	QUINTON Q-CATH, MODEL 000460
Applicant	Quinton, Inc.
Product code	DQK
Device class	Class II
Decision date	Sep 4, 2002
Decision	Substantially Equivalent
Regulation	870.1425

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View the full FDA submission: accessdata.fda.gov

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QUINTON Q-CATH, MODEL 000460

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