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VIVANT BREAST LESION LOCALIZATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K003439
510(k) Type
Traditional
Applicant
VIVANT MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/2000
Days to Decision
39 days
Submission Type
Summary

VIVANT BREAST LESION LOCALIZATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K003439
510(k) Type
Traditional
Applicant
VIVANT MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/2000
Days to Decision
39 days
Submission Type
Summary