Last synced on 30 November 2024 at 11:09 am

IN THE CANAL HEARING AID RC, REDICANAL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K843921
510(k) Type
Traditional
Applicant
OMNI HEARING SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/1984
Days to Decision
27 days