Olympus Integrated Endosurgery System Endoalpha (Control Unit for Endosurgery UCES-2) Software Version 2

FDA 510(k) K041494 · Olympus Corporation

Substantially Equivalent

510(k) numberK041494

Submission

Device name
Olympus Integrated Endosurgery System Endoalpha (Control Unit for Endosurgery UCES-2) Software Version 2
Applicant
Olympus Corporation
Melville, NY, US
Received
June 4, 2004
Decision date
July 1, 2004
Decision
Substantially Equivalent (SESE)
Type
Special 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 Olympus Integrated Endosurgery System Endoalpha (Control Unit for Endosurgery UCES-2) Software Version 2 cleared by the FDA?

Olympus Integrated Endosurgery System Endoalpha (Control Unit for Endosurgery UCES-2) Software Version 2 (K041494) received a 510(k) decision of Substantially Equivalent on July 1, 2004, 27 days after the submission was received.

What is the product code of K041494?

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.