Last synced on 25 January 2026 at 3:41 am

SENORX BIOPSY DEVICE, DRIVER, CONTROL MODULE, INCLUDING ACCESSORIES (POWER CORD,CONNECTOR CORDS AND FOOTSWITCH), VACUUMS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013641
510(k) Type
Traditional
Applicant
Senorx, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/2002
Days to Decision
85 days
Submission Type
Summary

SENORX BIOPSY DEVICE, DRIVER, CONTROL MODULE, INCLUDING ACCESSORIES (POWER CORD,CONNECTOR CORDS AND FOOTSWITCH), VACUUMS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013641
510(k) Type
Traditional
Applicant
Senorx, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/2002
Days to Decision
85 days
Submission Type
Summary