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RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 31108

Page Type
Cleared 510(K)
510(k) Number
K052506
510(k) Type
Special
Applicant
RUBICOR MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2005
Days to Decision
23 days
Submission Type
Summary

RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 31108

Page Type
Cleared 510(K)
510(k) Number
K052506
510(k) Type
Special
Applicant
RUBICOR MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/2005
Days to Decision
23 days
Submission Type
Summary