FDA 510(k)
FDA class 1
Substantially Equivalent
🇨🇭 Switzerland
Lyric4 Hearing Aid
K Number: K232999
·
Decision Apr 11, 2024
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
1366
Applicant Total
2
Review Days
202
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Basic Information
- Device Name
- Lyric4 Hearing Aid
- K Number
- K232999
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 874.3300
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Sonova AG
- Date Received
- September 22, 2023
- Decision Date
- April 11, 2024
- Product Code
- ESD
- Advisory Committee
- Ear, Nose, Throat
- Review Advisory Committee
- EN
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| ESD | Hearing Aid, Air-Conduction, Prescription | FDA class 1 | Ear, Nose, Throat |
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Other Clearances by Sonova AG
| K Number | Device Name | ||
|---|---|---|---|
| K230538 | All-Day Clear Slim ADCS1 Hearing Aid. All-Day Clear ADC1 Hearing Aid | Jun 16, 2023 | Substantially Equivalent |