Last synced on 25 January 2026 at 3:41 am

ARIETTA 50

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220295
510(k) Type
Abbreviated
Applicant
Fujifilm Healthcare Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
4/29/2022
Days to Decision
86 days
Submission Type
Summary

ARIETTA 50

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220295
510(k) Type
Abbreviated
Applicant
Fujifilm Healthcare Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
4/29/2022
Days to Decision
86 days
Submission Type
Summary