510(k) K963915

TELEX IN-THE-EAR CUSTOM HEARING AID WITH THRESHOLD COMPRESSION by Telex Communications, Inc. — Product Code ESD

K963915 is an FDA 510(k) premarket notification submitted by Telex Communications, Inc. for the device "TELEX IN-THE-EAR CUSTOM HEARING AID WITH THRESHOLD COMPRESSION". The FDA issued a decision of Substantially Equivalent on November 8, 1996. The device falls under product code ESD (Hearing Aid, Air-Conduction, Prescription), a Class I device regulated under 21 CFR 874.3300. Telex Communications, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 8, 1996
Date Received
September 30, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Hearing Aid, Air-Conduction, Prescription
Device Class
Class I
Regulation Number
874.3300
Review Panel
EN
Submission Type

An air-conduction hearing aid is a wearable sound amplifying device intended to compensate for impaired hearing that conducts sound to the ear through the air. This is a prescription hearing aid.