Last synced on 25 January 2026 at 3:41 am

INTEGRA, CUSTOM IN-THE-EAR HEARING AID

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K864180
510(k) Type
Traditional
Applicant
BERNAFON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1986
Days to Decision
9 days

INTEGRA, CUSTOM IN-THE-EAR HEARING AID

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K864180
510(k) Type
Traditional
Applicant
BERNAFON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1986
Days to Decision
9 days