Last synced on 30 November 2024 at 11:09 am

OTICON I22P CUSTOM FULL CONCHA (ITE) HRNG AID

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K893528
510(k) Type
Traditional
Applicant
OTICON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/1989
Days to Decision
99 days