Last synced on 14 November 2025 at 11:06 pm

Synapse 3D Perfusion Analysis

Page Type
Cleared 510(K)
510(k) Number
K162287
510(k) Type
Traditional
Applicant
FUJIFILM MEDICAL SYSTEMS U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/2017
Days to Decision
234 days
Submission Type
Summary

Synapse 3D Perfusion Analysis

Page Type
Cleared 510(K)
510(k) Number
K162287
510(k) Type
Traditional
Applicant
FUJIFILM MEDICAL SYSTEMS U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/2017
Days to Decision
234 days
Submission Type
Summary