Last synced on 4 February 2023 at 10:33 pm

BEHINDTHEEAR HEAR. AID MOD. 793U,M,UH,MH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K792334
510(k) Type
Traditional
Applicant
DANAVOX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/1979
Days to Decision
29 days