Last synced on 14 November 2025 at 11:06 pm

Mammomat Fusion with Stereotactic Biopsy

Page Type
Cleared 510(K)
510(k) Number
K163252
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2017
Days to Decision
53 days
Submission Type
Summary

Mammomat Fusion with Stereotactic Biopsy

Page Type
Cleared 510(K)
510(k) Number
K163252
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2017
Days to Decision
53 days
Submission Type
Summary