Last synced on 14 November 2025 at 11:06 pm

NeuroMatch

Page Type
Cleared 510(K)
510(k) Number
K250239
510(k) Type
Traditional
Applicant
LVIS Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2025
Days to Decision
116 days
Submission Type
Summary

NeuroMatch

Page Type
Cleared 510(K)
510(k) Number
K250239
510(k) Type
Traditional
Applicant
LVIS Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/23/2025
Days to Decision
116 days
Submission Type
Summary