FYD
- Product code
- FYD
- Device name
- Apparatus, Exhaust, Surgical
- Device class
- Class 2
- 21 CFR
- 21 CFR 878.5070
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 75
510(k) clearances, last 3 years (2)
| Number | Decision date | Applicant | Device name |
|---|---|---|---|
| K240127 | 2024-08-05 | Conmed Corporation | PlumeSafe X5 Smoke Management System summary |
| K233789 | 2024-04-10 | Surnic Corporation | 8Q10 Surclear Smoke Plume Evacuation System summary |
Official FDA classification page: FYD
Classification and pathway per current FDA publications. Data from openFDA (CC0).