Fujinon EPX-4440HD Digital Video Processor

FDA 510(k) K102466 · Fujinon, Inc.

Substantially Equivalent

510(k) numberK102466

Submission

Device name
Fujinon EPX-4440HD Digital Video Processor
Applicant
Fujinon, Inc.
Shelton, CT, US
Received
August 30, 2010
Decision date
May 25, 2011
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.

Other 510(k)s with product code FET

510(k)DeviceApplicantDecision
K2620794K Camera Head OLYMPUS CH-S700-08-LBFET · Traditional Olympus Medical Systems Corp.09/10/2026SE
K261880FUJIFILM Processor EP-8000;Balloon Controller PB-30;Endoscopy Support Program EW10-VM01FET · Special Fujifilm Corporation07/02/2026SE
K261260HD Camera Head OLYMPUS CH-S200-08-LBFET · Traditional Olympus Medical Systems Corporation06/24/2026SE
K251734ProVee Video Processing Unit (PV-003)FET · Traditional Proverum Limited09/24/2025SE
K250462UL UHD-Clear View 4K Camera System (UL-3Chip 4K)FET · Traditional Univlabs Technologies Private Limited08/11/2025SE
K250204Endoscopic Camera SystemFET · Traditional Shenzhen Sophway Technology Co., Ltd.07/01/2025SE
K243260FUJIFILM Processor EP-8000; FUJIFILM Endoscope Model EG-860RFET · Traditional Fujifilm Corporation04/11/2025SE
K242067Visera Elite III Video System Center Olympus OTV-S700; Visera Elite III LED Light Source…FET · Traditional Olympus Corporations of the Americas04/02/2025SE
K243321Endoscopic Video Image Processor (RP-IPD-V1000F)FET · Traditional Guangzhou Red Pine Medical Instrument Co., Ltd.02/07/2025SE
K241532Flexible Video-Choledo-Cysto-Ureteroscope System (PL-2100)FET · Traditional Shanghai SeeGen Photoelectric Technology Co., Ltd.10/22/2024SE

More from Shanghai SeeGen Photoelectric Technology Co., Ltd.

510(k)DeviceDecision
K120446Fujinon/Fujifilm Ultrasonic Endoscope EG-530UR2 and EG-530UT2FDS · Traditional 08/13/2012SE
K112391Fujinon ColonoscopesFDF · Special 07/26/2012SE
K111243Fujinon Ultrasonic ProcessorFDS · Special 05/16/2011SE
K091773Fujinon Sterile OvertubesFED · Special 08/07/2009SE
K090116Fujinon Colonoscope for Double Balloon Enterscopy System Model, EC-450B15FDF · Traditional 04/22/2009SE
K063316Fujinon Model EG-530N Trans Nasal InsertionFDS · Traditional 03/16/2007SE
K063847Fujinon Ultrasonic Endoscope and Processor, Models EG-530UR, EG-530UT and SU-700FDS · Traditional 03/01/2007SE
K050907Fujinon G5 Bronchoscopes, Models EB-470S, EB-250S, and EB-270PEOQ · Traditional 05/19/2005SE
K042043Fujinon Inc. G5 Gastroscopes, Models EC-450WR5, EC-250WR5FDS · Traditional 11/24/2004SE
K042076Fujinon G5 Duodenscopes; G5 Duodenoscopes, ED-450XT5, ED-250XT5FDT · Traditional 11/18/2004SE

Questions and answers

When was Fujinon EPX-4440HD Digital Video Processor cleared by the FDA?

Fujinon EPX-4440HD Digital Video Processor (K102466) received a 510(k) decision of Substantially Equivalent on May 25, 2011, 268 days after the submission was received.

What is the product code of K102466?

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.