Last synced on 2 December 2022 at 11:04 pm

Desyncra for Tinnitus Therapy System, Desyncra for Tinnitus Pro System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151558
510(k) Type
Traditional
Applicant
NEUROTHERAPIES RESET GMBH.
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
1/20/2016
Days to Decision
224 days
Submission Type
Statement

Desyncra for Tinnitus Therapy System, Desyncra for Tinnitus Pro System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151558
510(k) Type
Traditional
Applicant
NEUROTHERAPIES RESET GMBH.
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
1/20/2016
Days to Decision
224 days
Submission Type
Statement