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SYNAPSE 3D BASE TOOLS

Page Type
Cleared 510(K)
510(k) Number
K120361
510(k) Type
Traditional
Applicant
FUJIFILM MEDICAL SYSTEMS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/2012
Days to Decision
60 days
Submission Type
Summary

SYNAPSE 3D BASE TOOLS

Page Type
Cleared 510(K)
510(k) Number
K120361
510(k) Type
Traditional
Applicant
FUJIFILM MEDICAL SYSTEMS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/2012
Days to Decision
60 days
Submission Type
Summary