FUJIFILM Endoscope Model EB-710XT— 510(k) K240075
Substantially EquivalentFUJIFILM Healthcare Americas Corporation
FDA 510(k) clearance K240075 for FUJIFILM Endoscope Model EB-710XT, Substantially Equivalent on 2024-02-07. Applicant: FUJIFILM Healthcare Americas Corporation. Device class: 2.
Clearance details
- Applicant
- FUJIFILM Healthcare Americas Corporation
- Product code
- Product code EOQ
- Device class
- Class 2
- Regulation
- 21 CFR 874.4680
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Lexington, MA, US
Recent devices under product code EOQ
view allMore clearances from FUJIFILM Healthcare Americas Corporation
view allAdverse events under product code EOQ
product code EOQ- Death
- 135
- Injury
- 2,863
- Malfunction
- 21,662
- Total
- 24,660
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.