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WAVi™ Headset and WAVi™ eSoc™ Single Use Electrode Contacts

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162460
510(k) Type
Traditional
Applicant
Wavi Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/2017
Days to Decision
238 days
Submission Type
Summary

WAVi™ Headset and WAVi™ eSoc™ Single Use Electrode Contacts

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162460
510(k) Type
Traditional
Applicant
Wavi Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/2017
Days to Decision
238 days
Submission Type
Summary