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EEG Electrode Template

Page Type
Cleared 510(K)
510(k) Number
K191225
510(k) Type
Traditional
Applicant
Rhythmlink International, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2019
Days to Decision
90 days
Submission Type
Summary

EEG Electrode Template

Page Type
Cleared 510(K)
510(k) Number
K191225
510(k) Type
Traditional
Applicant
Rhythmlink International, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2019
Days to Decision
90 days
Submission Type
Summary