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SENOSONIX ULTRASOUND BREAST BIOPSY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K072541
510(k) Type
Traditional
Applicant
SENORX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/2007
Days to Decision
15 days
Submission Type
Summary

SENOSONIX ULTRASOUND BREAST BIOPSY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K072541
510(k) Type
Traditional
Applicant
SENORX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/2007
Days to Decision
15 days
Submission Type
Summary