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TA-641 TINNITUS INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K800702
510(k) Type
Traditional
Applicant
AUDIOTRONE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/1980
Days to Decision
41 days

TA-641 TINNITUS INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K800702
510(k) Type
Traditional
Applicant
AUDIOTRONE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/1980
Days to Decision
41 days