K-number	K070311
Device name	CARDIOBLATE GEMINI SURGICAL ABLATION DEVICE, MODELS 49260 AND 49261
Applicant	Medtronic Vascular
Product code	GEI
Device class	Class II
Decision date	Apr 24, 2007
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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CARDIOBLATE GEMINI SURGICAL ABLATION DEVICE, MODELS 49260 AND 49261

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