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IN-THE-EAR MODEL 821

Page Type
Cleared 510(K)
510(k) Number
K812938
510(k) Type
Traditional
Applicant
DANAVOX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/1981
Days to Decision
17 days

IN-THE-EAR MODEL 821

Page Type
Cleared 510(K)
510(k) Number
K812938
510(k) Type
Traditional
Applicant
DANAVOX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/1981
Days to Decision
17 days