K251807
- 510(k) number
- K251807
- Device name
- Single Use Electrosurgical Hemostatic Forceps FD-410LR, FD-411UR, FD-412LR
- Applicant
- Olympus Medical Systems Corp. JP
- Product code
- KGE — Forceps, Biopsy, Electric
- Decision date
- 2026-03-06
- Date received
- 2025-06-12
- 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: K251807.pdf
Official FDA record: K251807
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.