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RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30629

Page Type
Cleared 510(K)
510(k) Number
K032584
510(k) Type
Special
Applicant
RUBICOR MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/2003
Days to Decision
27 days
Submission Type
Summary

RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30629

Page Type
Cleared 510(K)
510(k) Number
K032584
510(k) Type
Special
Applicant
RUBICOR MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/2003
Days to Decision
27 days
Submission Type
Summary