Last synced on 30 September 2022 at 11:05 pm

WIDEX MODEL LX-ITE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K944838
510(k) Type
Traditional
Applicant
WIDEX HEARING AID CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/1994
Days to Decision
20 days
Submission Type
Statement