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TinniLogic Mobile Tinnitus Management Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163094
510(k) Type
Traditional
Applicant
JIANGSU BETTERLIFE MEDICAL CO., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/17/2017
Days to Decision
194 days
Submission Type
Summary

TinniLogic Mobile Tinnitus Management Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163094
510(k) Type
Traditional
Applicant
JIANGSU BETTERLIFE MEDICAL CO., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/17/2017
Days to Decision
194 days
Submission Type
Summary