K232999
- 510(k) number
- K232999
- Device name
- Lyric4 Hearing Aid
- Applicant
- Sonova AG CH
- Product code
- ESD — Hearing Aid, Air-Conduction, Prescription
- Decision date
- 2024-04-11
- Date received
- 2023-09-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ear, Nose, Throat
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K232999.pdf
Official FDA record: K232999
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.