K251692
- 510(k) number
- K251692
- Device name
- Advanced Tissue Resection Device
- Applicant
- Micro-Tech (Nanjing) Co., Ltd. CN
- Product code
- FDI — Snare, Flexible
- Decision date
- 2026-02-21
- Date received
- 2025-06-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
510(k) Summary (official FDA PDF): K251692.pdf
Official FDA record: K251692
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.