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ASPIRE HD FULL-FIELD DIGITAL MAMMOGRAPHY SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110729
510(k) Type
Traditional
Applicant
Fujifilm Medical Systems U.S.A, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/2011
Days to Decision
169 days
Submission Type
Summary

ASPIRE HD FULL-FIELD DIGITAL MAMMOGRAPHY SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110729
510(k) Type
Traditional
Applicant
Fujifilm Medical Systems U.S.A, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/2011
Days to Decision
169 days
Submission Type
Summary