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RUBICOR MAGIC BREAST BIOPSY DEVICE, MODEL 31537

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071048
510(k) Type
Special
Applicant
RUBICOR MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2007
Days to Decision
32 days
Submission Type
Summary

RUBICOR MAGIC BREAST BIOPSY DEVICE, MODEL 31537

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071048
510(k) Type
Special
Applicant
RUBICOR MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2007
Days to Decision
32 days
Submission Type
Summary