OTICON
Hearing Aid, Air Conduction
OTICON, INC.
The following data is part of a premarket notification filed by Oticon, Inc. with the FDA for Oticon.
Pre-market Notification Details
| Device ID | K954794 |
| 510k Number | K954794 |
| Device Name: | OTICON |
| Classification | Hearing Aid, Air Conduction |
| Applicant | OTICON, INC. 29 SCHOOLHOUSE RD. Somerset, NJ 08873 |
| Contact | Preben Brunved |
| Correspondent | Preben Brunved OTICON, INC. 29 SCHOOLHOUSE RD. 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 | 1995-10-18 |
| Decision Date | 1995-11-13 |
Trademark Results [OTICON]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 OTICON 79079647 3916258 Live/Registered |
Oticon A/S 2010-01-28 |
 OTICON 77921607 4023465 Live/Registered |
Oticon A/S 2010-01-27 |
 OTICON 76220440 2655786 Live/Registered |
Oticon A/S 2001-03-06 |
 OTICON 73086309 1103330 Dead/Expired |
OTICON ELECTRONICS 1976-05-06 |
 OTICON 73013700 1021986 Dead/Expired |
OTICON ELECTRONICS, A/S 1974-02-19 |
 OTICON 71666965 0600081 Dead/Expired |
LEHMAN, CHARLES H. 1954-05-24 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.