Last synced on 2 December 2022 at 11:04 pm

TELEX IN-THE-EAR CUSTOM HEARING AID WITH THRESHOLD COMPRESSION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963915
510(k) Type
Traditional
Applicant
TELEX COMMUNICATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/8/1996
Days to Decision
39 days
Submission Type
Summary