K-number	K032047
Device name	TRI-LOOP MICROWAVE ABLATION PROBE
Applicant	Vivant Medical, Inc.
Product code	GEI
Device class	Class II
Decision date	Aug 6, 2003
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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TRI-LOOP MICROWAVE ABLATION PROBE

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