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HISONIC-TRD TINNITUS RELIEF DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013253
510(k) Type
Traditional
Applicant
HEARING INNOVATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/2002
Days to Decision
189 days
Submission Type
Summary

HISONIC-TRD TINNITUS RELIEF DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013253
510(k) Type
Traditional
Applicant
HEARING INNOVATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/2002
Days to Decision
189 days
Submission Type
Summary