Last synced on 25 November 2022 at 11:04 pm

TINNITUS MASKERS MODEL S584

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790190
510(k) Type
Traditional
Applicant
VICAN INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1979
Days to Decision
17 days

TINNITUS MASKERS MODEL S584

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K790190
510(k) Type
Traditional
Applicant
VICAN INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1979
Days to Decision
17 days