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SYNAPSE 3D NODULE ANALYSIS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120679
510(k) Type
Traditional
Applicant
FUJIFILM MEDICAL SYSTEMS U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/2012
Days to Decision
87 days
Submission Type
Summary

SYNAPSE 3D NODULE ANALYSIS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120679
510(k) Type
Traditional
Applicant
FUJIFILM MEDICAL SYSTEMS U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/2012
Days to Decision
87 days
Submission Type
Summary