K-number	K041340
Device name	GUIDANT MICROWAVE ABLATION SYSTEM
Applicant	Guidant Corporation, Cardiac Surgery
Product code	NEY
Device class	Class II
Decision date	Jul 28, 2004
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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GUIDANT MICROWAVE ABLATION SYSTEM

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