Visera Elite II Video System Center, Visera Elite II Endoeye 3D

FDA 510(k) K193026 · Olympus Medical Systems Corp.

Substantially Equivalent

510(k) numberK193026

Submission

Device name
Visera Elite II Video System Center, Visera Elite II Endoeye 3D
Applicant
Olympus Medical Systems Corp.
Hachioji-Shi, JP
Received
October 30, 2019
Decision date
April 3, 2020
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GCJ – Laparoscope, General & Plastic Surgery
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

Other 510(k)s with product code GCJ

510(k)DeviceApplicantDecision
K262397CuratOR EX2742GCJ · Traditional Eizo Corporation09/11/2026SE
K260884UNIDRIVE Select SystemGCJ · Traditional Karl Storz SE & CO. KG09/01/2026SE
K260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorGCJ · Traditional Sony Corporation08/26/2026SE
K261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)GCJ · Traditional Freyja Healthcare, LLC08/13/2026SE
K253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ…GCJ · Traditional Medical Impact07/24/2026SE
K261614LED LCD Monitor (OEV-271H)GCJ · Traditional Lg Electronics.Inc07/17/2026SE
K261249Universal Seal (5-12 mm)GCJ · Traditional Intuitive Surgical, Inc.07/14/2026SE
K260710FloShield Air System (FSS-01-1000T - 10mm, 0 Degree FloShield Air, FSS-02-1030T - 10mm…GCJ · Traditional FloShield, Inc.06/11/2026SE
K260414“Tech-Image” Video Endoscope SystemGCJ · Traditional Tech-Image CO., LTD.06/10/2026SE
K253994TroKit Laparoscope Lens WiperGCJ · Traditional TroCare, LLC06/04/2026SE

More from TroCare, LLC

510(k)DeviceDecision
K2620794K Camera Head OLYMPUS CH-S700-08-LBFET · Traditional 09/10/2026SE
K260856Disposable Distal Attachment D-201-13404FDS · Traditional 08/27/2026SE
K260824Gastrointestinal Videoscope Olympus GIF-2T1500FDS · Traditional 08/27/2026SE
K260401Evis Eus Ultrasound Bronchofibervideoscope Olympus BF-UCP190F (BF-UCP190F)PSV · Traditional 08/27/2026SE
K261183EVIS EUS Ultrasound Gastrointestinal Videoscope (Olympus GF-UE190)ODG · Traditional 07/31/2026SE
K254056THUNDERBEAT 5 mm, 45 cm, Front-actuated Grip Type S (TB-0545FCS); THUNDERBEAT 5 mm, 35…GEI · Traditional 07/01/2026SE
K261260HD Camera Head OLYMPUS CH-S200-08-LBFET · Traditional 06/24/2026SE
K260580Single Use Reloadable Clip Applicator (HX-810LR, HX-810UR); Clip (HX-610-090…PKL · Traditional 05/21/2026SE
K252341Evis Exera III Bronchovideoscope (Olympus BF-Q190); Evis Exera III Bronchovideoscope…EOQ · Traditional 04/23/2026SE
K252050Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241DEOB · Traditional 03/20/2026SE

Questions and answers

When was Visera Elite II Video System Center, Visera Elite II Endoeye 3D cleared by the FDA?

Visera Elite II Video System Center, Visera Elite II Endoeye 3D (K193026) received a 510(k) decision of Substantially Equivalent on April 3, 2020, 156 days after the submission was received.

What is the product code of K193026?

The FDA product code is GCJ – Laparoscope, General & Plastic Surgery, a Class II (moderate risk) device regulated under 21 CFR 876.1500.