K-number	K992479
Device name	ENSITE 3000 SYSTEM
Applicant	Endocardial Solutions, Inc.
Product code	DQK
Device class	Class II
Decision date	Dec 2, 1999
Decision	Unknown
Regulation	870.1425

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Source

View the full FDA submission: accessdata.fda.gov

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ENSITE 3000 SYSTEM

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