K244017
- 510(k) number
- K244017
- Device name
- FUJIFILM Endoscope Model EB-710P; FUJIFILM Processor EP-8000
- Applicant
- Fujifilm Corporation JP
- Product code
- EOQ — Bronchoscope (Flexible Or Rigid)
- Decision date
- 2025-06-13
- Date received
- 2024-12-27
- 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: K244017.pdf
Official FDA record: K244017
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.