Last synced on 10 January 2025 at 11:05 pm

NEUROMARK System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222032
510(k) Type
Traditional
Applicant
Neurent Medical
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
10/26/2022
Days to Decision
107 days
Submission Type
Summary

NEUROMARK System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222032
510(k) Type
Traditional
Applicant
Neurent Medical
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
10/26/2022
Days to Decision
107 days
Submission Type
Summary