K-number	K003439
Device name	VIVANT BREAST LESION LOCALIZATION DEVICE
Applicant	Vivant Medical, Inc.
Product code	KNW
Device class	Class II
Decision date	Dec 15, 2000
Decision	Substantially Equivalent
Regulation	876.1075

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View the full FDA submission: accessdata.fda.gov

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VIVANT BREAST LESION LOCALIZATION DEVICE

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