Last synced on 14 November 2025 at 11:06 pm

22MM SITESELECT BREAST BIOPSY DEVICE MODEL SSD022

Page Type
Cleared 510(K)
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)
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