K242857
- 510(k) number
- K242857
- Device name
- ClearHemograsper
- Applicant
- Finemedix Co., Ltd. KR
- Product code
- KGE — Forceps, Biopsy, Electric
- Decision date
- 2025-05-21
- Date received
- 2024-09-20
- 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: K242857.pdf
Official FDA record: K242857
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.