Last synced on 25 January 2026 at 3:41 am

Synapse Enterprise Viewer Version 1.0

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183248
510(k) Type
Traditional
Applicant
Fujifilm Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
4/25/2019
Days to Decision
155 days
Submission Type
Summary

Synapse Enterprise Viewer Version 1.0

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K183248
510(k) Type
Traditional
Applicant
Fujifilm Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
4/25/2019
Days to Decision
155 days
Submission Type
Summary