Last synced on 14 November 2025 at 11:06 pm

Desyncra for Tinnitus Therapy System, Desyncra for Tinnitus Pro System

Page Type
Cleared 510(K)
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)
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