FUJIFILM Processor EP-8000; FUJIFILM Endoscope Model EG-860R

FDA 510(k) K243260 · Fujifilm Corporation

Substantially Equivalent

510(k) numberK243260

Submission

Device name
FUJIFILM Processor EP-8000; FUJIFILM Endoscope Model EG-860R
Applicant
Fujifilm Corporation
Ashigara Kami-Gun, JP
Received
October 15, 2024
Decision date
April 11, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FET – Endoscopic Video Imaging System/Component, Gastroenterology-Urology
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

To allow for visualization of body cavities through an endoscope by projecting images to a monitor.

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Questions and answers

When was FUJIFILM Processor EP-8000; FUJIFILM Endoscope Model EG-860R cleared by the FDA?

FUJIFILM Processor EP-8000; FUJIFILM Endoscope Model EG-860R (K243260) received a 510(k) decision of Substantially Equivalent on April 11, 2025, 178 days after the submission was received.

What is the product code of K243260?

The FDA product code is FET – Endoscopic Video Imaging System/Component, Gastroenterology-Urology, a Class II (moderate risk) device regulated under 21 CFR 876.1500.