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MODIFICATION TO RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30086

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030049
510(k) Type
Special
Applicant
RUBICOR MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/2003
Days to Decision
23 days
Submission Type
Summary

MODIFICATION TO RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30086

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030049
510(k) Type
Special
Applicant
RUBICOR MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/2003
Days to Decision
23 days
Submission Type
Summary