Last synced on 25 January 2026 at 3:41 am

Sentimag System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222832
510(k) Type
Traditional
Applicant
Endomagnetics Ltd.,
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/21/2023
Days to Decision
123 days
Submission Type
Summary

Sentimag System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222832
510(k) Type
Traditional
Applicant
Endomagnetics Ltd.,
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/21/2023
Days to Decision
123 days
Submission Type
Summary