The following data is part of a premarket notification filed by Audifon-usa Inc. with the FDA for An Evo 1, Cs Evo 1, Contact Mini, Apollon.
| Device ID | K121793 |
| 510k Number | K121793 |
| Device Name: | AN EVO 1, CS EVO 1, CONTACT MINI, APOLLON |
| Classification | Hearing Aid, Bone Conduction |
| Applicant | AUDIFON-USA INC. 403 CHAIRMAN CT., STE. 1 Debary, FL 32713 |
| Contact | Jane E Perrone |
| Correspondent | Jane E Perrone AUDIFON-USA INC. 403 CHAIRMAN CT., STE. 1 Debary, FL 32713 |
| Product Code | LXB |
| CFR Regulation Number | 874.3300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-06-19 |
| Decision Date | 2012-11-01 |
| Summary: | summary |