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RUBICOR MAGIC BREAST BIOPSY DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K053151
510(k) Type
Traditional
Applicant
Rubicor Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/2005
Days to Decision
8 days
Submission Type
Summary

RUBICOR MAGIC BREAST BIOPSY DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K053151
510(k) Type
Traditional
Applicant
Rubicor Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/2005
Days to Decision
8 days
Submission Type
Summary