Last synced on 20 December 2024 at 11:05 pm

Synapse 3D Perfusion Analysis

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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