Last synced on 25 November 2022 at 11:04 pm

SoundCure Serenade Tinnitus Treatment System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150065
510(k) Type
Traditional
Applicant
SoundCure, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2015
Days to Decision
90 days
Submission Type
Summary

SoundCure Serenade Tinnitus Treatment System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K150065
510(k) Type
Traditional
Applicant
SoundCure, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2015
Days to Decision
90 days
Submission Type
Summary