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NeuroOne Cortical Electrode

Page Type
Cleared 510(K)
510(k) Number
K192764
510(k) Type
Traditional
Applicant
NeuroOne, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/2019
Days to Decision
57 days
Submission Type
Summary

NeuroOne Cortical Electrode

Page Type
Cleared 510(K)
510(k) Number
K192764
510(k) Type
Traditional
Applicant
NeuroOne, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/2019
Days to Decision
57 days
Submission Type
Summary