K231721
- 510(k) number
- K231721
- Device name
- Disposable Hot Biopsy Forceps
- Applicant
- Beijing Zksk Technology Co., Ltd. CN
- Product code
- KGE — Forceps, Biopsy, Electric
- Decision date
- 2023-12-14
- Date received
- 2023-06-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 3.2 MB · U.S. public domain
Also available from FDA: K231721.pdf
Official FDA record: K231721
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.