MYE
- Product code
- MYE
- Device name
- System, Electrogastrography (Egg)
- Device class
- Class 2
- 21 CFR
- 21 CFR 876.1735
- Medical specialty
- Gastroenterology, Urology
- Marketing pathway
- 510(K)
- 510(k) clearances (last 3 years)
- 3
- Summaries archived here
- 3 (direct download)
- 510(k) clearances (all years, FDA)
- 8 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (3)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K252504 | 2025-12-05 | Alimetry , Ltd. | Gastric Alimetry | |
| K240946 | 2024-07-03 | Alimetry , Ltd. | Gastric Alimetry | |
| K232925 | 2023-11-17 | Alimetry , Ltd. | Gastric Alimetry System |
Official FDA classification page: MYE
Classification and pathway per current FDA publications. Data from openFDA (CC0).