K250187
- 510(k) number
- K250187
- Device name
- Disposable Hot Biopsy Forceps (FD-210U); Disposable Hot Biopsy Forceps (FD-230U)
- Applicant
- Olympus Medical Systems Corporation JP
- Product code
- KGE — Forceps, Biopsy, Electric
- Decision date
- 2025-10-07
- Date received
- 2025-01-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K250187.pdf
Official FDA record: K250187
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.