FDI
- Product code
- FDI
- Device name
- Snare, Flexible
- Device class
- Class 2
- 21 CFR
- 21 CFR 876.4300
- Medical specialty
- Gastroenterology, Urology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 1
- Summaries archived here
- 0 (direct download)
- 510(k) clearances (all years, FDA)
- 63 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K251692 | 2026-02-21 | Micro-Tech (Nanjing) Co., Ltd. | Advanced Tissue Resection Device | FDA |
Official FDA classification page: FDI
Classification and pathway per current FDA publications. Data from openFDA (CC0).