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CUSTOM IN-THE-EAR HEARING AID OTICON MODEL: P

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902559
510(k) Type
Traditional
Applicant
OTICON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/1990
Days to Decision
28 days