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

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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