K-number	K061865
Device name	FLEX 10 MIS ABLATION PROBE, MODEL FLX10MI-05
Applicant	Guidant Corp.
Product code	NEY
Device class	Class II
Decision date	Jul 27, 2006
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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FLEX 10 MIS ABLATION PROBE, MODEL FLX10MI-05

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