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 |