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SYNAPSE 3D CARDIAC TOOLS

Page Type
Cleared 510(K)
510(k) Number
K103465
510(k) Type
Traditional
Applicant
FUJIFILM MEDICAL SYSTEMS U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/2011
Days to Decision
68 days
Submission Type
Summary

SYNAPSE 3D CARDIAC TOOLS

Page Type
Cleared 510(K)
510(k) Number
K103465
510(k) Type
Traditional
Applicant
FUJIFILM MEDICAL SYSTEMS U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/2011
Days to Decision
68 days
Submission Type
Summary