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Tinnitogram Signal Generator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221168
510(k) Type
Traditional
Applicant
Goldenear Company, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/2023
Days to Decision
285 days
Submission Type
Summary

Tinnitogram Signal Generator

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221168
510(k) Type
Traditional
Applicant
Goldenear Company, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/1/2023
Days to Decision
285 days
Submission Type
Summary