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TINNITUS PHASE-OUT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061111
510(k) Type
Special
Applicant
TINNITUS CONTROL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/2006
Days to Decision
25 days
Submission Type
Summary

TINNITUS PHASE-OUT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K061111
510(k) Type
Special
Applicant
TINNITUS CONTROL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/2006
Days to Decision
25 days
Submission Type
Summary