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RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30086

Page Type
Cleared 510(K)
510(k) Number
K023601
510(k) Type
Special
Applicant
RUBICOR MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2002
Days to Decision
22 days
Submission Type
Summary

RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30086

Page Type
Cleared 510(K)
510(k) Number
K023601
510(k) Type
Special
Applicant
RUBICOR MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2002
Days to Decision
22 days
Submission Type
Summary