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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
K111293
510(k) Type
Traditional
Applicant
SOUNDCURE INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2011
Days to Decision
110 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
K111293
510(k) Type
Traditional
Applicant
SOUNDCURE INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2011
Days to Decision
110 days
Submission Type
Summary