Last synced on 24 May 2024 at 11:04 pm

ECHELON Synergy V10.0

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233687
510(k) Type
Traditional
Applicant
Fujifilm Healthcare Americas Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2024
Days to Decision
168 days
Submission Type
Summary

ECHELON Synergy V10.0

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233687
510(k) Type
Traditional
Applicant
Fujifilm Healthcare Americas Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2024
Days to Decision
168 days
Submission Type
Summary