K233772
- 510(k) number
- K233772
- Device name
- Disposable Dual Action Tissue Closure Device
- Applicant
- Mirco-Tech (Nanjing) Co., Ltd. CN
- Product code
- PKL — Hemostatic Metal Clip For The Gi Tract
- Decision date
- 2024-03-19
- Date received
- 2023-11-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K233772.pdf
Official FDA record: K233772
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.