Last synced on 14 November 2025 at 11:06 pm

NEUROMARK System

Page Type
Cleared 510(K)
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)
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