The following data is part of a premarket notification filed by Telex Communications, Inc. with the FDA for Telex 349 Multi Cros W/adapive Compression.
Device ID | K954579 |
510k Number | K954579 |
Device Name: | TELEX 349 MULTI CROS W/ADAPIVE COMPRESSION |
Classification | Hearing Aid, Air Conduction |
Applicant | TELEX COMMUNICATIONS, INC. 9600 ALDRICH AVENUE SOUTH Minneapolis, MN 55420 |
Contact | Tom Scheller |
Correspondent | Tom Scheller TELEX COMMUNICATIONS, INC. 9600 ALDRICH AVENUE SOUTH Minneapolis, MN 55420 |
Product Code | ESD |
CFR Regulation Number | 874.3300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-10-02 |
Decision Date | 1995-12-08 |