Last synced on 24 January 2025 at 11:04 pm

Neuromark System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212666
510(k) Type
Traditional
Applicant
Neurent Medical
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
10/22/2021
Days to Decision
60 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
K212666
510(k) Type
Traditional
Applicant
Neurent Medical
Country
Ireland
FDA Decision
Substantially Equivalent
Decision Date
10/22/2021
Days to Decision
60 days
Submission Type
Summary