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TINNITUS DEVICES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790064
510(k) Type
Traditional
Applicant
VICON INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/16/1979
Days to Decision
32 days

TINNITUS DEVICES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790064
510(k) Type
Traditional
Applicant
VICON INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/16/1979
Days to Decision
32 days