K252271
- 510(k) number
- K252271
- Device name
- Hemoclip
- Applicant
- Hangzhou AGS MedTech Co., Ltd. CN
- Product code
- PKL — Hemostatic Metal Clip For The Gi Tract
- Decision date
- 2025-11-12
- Date received
- 2025-07-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K252271.pdf
Official FDA record: K252271
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.