Last synced on 19 July 2024 at 11:05 pm

TINNITUS MASKER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K781798
510(k) Type
Traditional
Applicant
STARKEY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1978
Days to Decision
11 days

TINNITUS MASKER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K781798
510(k) Type
Traditional
Applicant
STARKEY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1978
Days to Decision
11 days