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TINNITUS SOUND GENERATOR MODULE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110932
510(k) Type
Special
Applicant
Gn Resound A/S
Country
Denmark
FDA Decision
Substantially Equivalent
Decision Date
5/3/2011
Days to Decision
29 days
Submission Type
Summary

TINNITUS SOUND GENERATOR MODULE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110932
510(k) Type
Special
Applicant
Gn Resound A/S
Country
Denmark
FDA Decision
Substantially Equivalent
Decision Date
5/3/2011
Days to Decision
29 days
Submission Type
Summary