Last synced on 12 July 2024 at 11:04 pm

APERTO Lucent MRI System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233629
510(k) Type
Traditional
Applicant
FUJIFILM Healthcare Americas Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/2024
Days to Decision
179 days
Submission Type
Summary

APERTO Lucent MRI System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233629
510(k) Type
Traditional
Applicant
FUJIFILM Healthcare Americas Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/2024
Days to Decision
179 days
Submission Type
Summary