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 |