K240075
- 510(k) number
- K240075
- Device name
- FUJIFILM Endoscope Model EB-710XT
- Applicant
- FUJIFILM Healthcare Americas Corporation MA · US
- Product code
- EOQ — Bronchoscope (Flexible Or Rigid)
- Decision date
- 2024-02-07
- Date received
- 2024-01-10
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Ear, Nose, Throat
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K240075.pdf
Official FDA record: K240075
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.