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BREAST IMMOBIIZATION AND BIOPSY DEVICE MR-BIOPSY 160

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010570
510(k) Type
Traditional
Applicant
Mri Devices Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2001
Days to Decision
42 days
Submission Type
Statement

BREAST IMMOBIIZATION AND BIOPSY DEVICE MR-BIOPSY 160

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010570
510(k) Type
Traditional
Applicant
Mri Devices Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2001
Days to Decision
42 days
Submission Type
Statement