K252050
- 510(k) number
- K252050
- Device name
- Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D
- Applicant
- Olympus Medical Systems Corporation JP
- Product code
- EOB — Nasopharyngoscope (Flexible Or Rigid)
- Decision date
- 2026-03-20
- Date received
- 2025-07-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ear, Nose, Throat
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K252050.pdf
Official FDA record: K252050
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.