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CONFIRMA BREAST MRI INTERVENTIONAL COMPONENTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071534
510(k) Type
Traditional
Applicant
CONFIRMA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/2007
Days to Decision
34 days
Submission Type
Summary

CONFIRMA BREAST MRI INTERVENTIONAL COMPONENTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071534
510(k) Type
Traditional
Applicant
CONFIRMA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/2007
Days to Decision
34 days
Submission Type
Summary