The following data is part of a premarket notification filed by Electone, Inc. with the FDA for Electone Bte Model Am 240 Hf.
Device ID | K910099 |
510k Number | K910099 |
Device Name: | ELECTONE BTE MODEL AM 240 HF |
Classification | Hearing Aid, Air Conduction |
Applicant | ELECTONE, INC. P.O. BOX 910 Winter Park, FL 32790 |
Contact | Jim Nee |
Correspondent | Jim Nee ELECTONE, INC. P.O. BOX 910 Winter Park, FL 32790 |
Product Code | ESD |
CFR Regulation Number | 874.3300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-01-09 |
Decision Date | 1991-01-29 |