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22MM SITESELECT BREAST BIOPSY DEVICE MODEL SSD022

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011575
510(k) Type
Traditional
Applicant
Imagyn Surgical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/2001
Days to Decision
87 days
Submission Type
Summary

22MM SITESELECT BREAST BIOPSY DEVICE MODEL SSD022

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011575
510(k) Type
Traditional
Applicant
Imagyn Surgical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/2001
Days to Decision
87 days
Submission Type
Summary