Last synced on 30 November 2024 at 11:09 am

Q21

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221959
510(k) Type
Traditional
Applicant
NeuroField Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/2023
Days to Decision
422 days
Submission Type
Summary

Q21

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221959
510(k) Type
Traditional
Applicant
NeuroField Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/2023
Days to Decision
422 days
Submission Type
Summary