Last synced on 14 November 2025 at 11:06 pm

RUBICOR MAGIC BREAST BIOPSY DEVICE, MODEL 31537

Page Type
Cleared 510(K)
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)
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