The following data is part of a premarket notification filed by Audifon-usa Inc. with the FDA for Audifon Arriva Cic, Is, Is+, M, S, S+, X Trt, Audifon Vico, Audifon Prado, Audifon Elia, Cic, Is, Is+, M, S Trt.
| Device ID | K130514 | 
| 510k Number | K130514 | 
| Device Name: | AUDIFON ARRIVA CIC, IS, IS+, M, S, S+, X TRT, AUDIFON VICO, AUDIFON PRADO, AUDIFON ELIA, CIC, IS, IS+, M, S TRT | 
| Classification | Masker, Tinnitus | 
| Applicant | AUDIFON-USA INC. 403 CHAIRMAN COURT, STE. 1 Debary, FL 32713 | 
| Contact | Jane E Perrone | 
| Correspondent | Jane E Perrone AUDIFON-USA INC. 403 CHAIRMAN COURT, STE. 1 Debary, FL 32713 | 
| Product Code | KLW | 
| CFR Regulation Number | 874.3400 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Abbreviated | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2013-02-27 | 
| Decision Date | 2013-11-21 | 
| Summary: | summary |