Last synced on 6 December 2024 at 11:05 pm

OTICON E28A

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K841436
510(k) Type
Traditional
Applicant
OTICON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/1984
Days to Decision
82 days