Last synced on 25 April 2025 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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