The following data is part of a premarket notification filed by Oticon Corp. with the FDA for Oticon Bte Hearing Aid (behind-the-ear), Model E44.
Device ID | K901292 |
510k Number | K901292 |
Device Name: | OTICON BTE HEARING AID (BEHIND-THE-EAR), MODEL E44 |
Classification | Hearing Aid, Air Conduction |
Applicant | OTICON CORP. 29 SCHOOLHOUSE RD. P.O. BOX 6724 Somerset, NJ 08873 |
Contact | Preben Brunved |
Correspondent | Preben Brunved OTICON CORP. 29 SCHOOLHOUSE RD. P.O. BOX 6724 Somerset, NJ 08873 |
Product Code | ESD |
CFR Regulation Number | 874.3300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-03-20 |
Decision Date | 1990-04-10 |