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SYNAPSE 3D CARDIAC TOOLS

Page Type
Cleared 510(K)
510(k) Number
K130383
510(k) Type
Traditional
Applicant
FUJIFILM MEDICAL SYSTEM U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2013
Days to Decision
54 days
Submission Type
Summary

SYNAPSE 3D CARDIAC TOOLS

Page Type
Cleared 510(K)
510(k) Number
K130383
510(k) Type
Traditional
Applicant
FUJIFILM MEDICAL SYSTEM U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2013
Days to Decision
54 days
Submission Type
Summary