Visera S Video System Center Olympus OTV-S500 (Olympus OTV-S500)

FDA 510(k) K243380 · Olympus Medical Systems Corporation

Substantially Equivalent

510(k) numberK243380

Submission

Device name
Visera S Video System Center Olympus OTV-S500 (Olympus OTV-S500)
Applicant
Olympus Medical Systems Corporation
Hachioji-Shi, JP
Received
October 30, 2024
Decision date
March 3, 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
EOB – Nasopharyngoscope (Flexible Or Rigid)
Device class
Class II (moderate risk)
Regulation
21 CFR 874.4760
Specialty
Ear, Nose, Throat

If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (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 EOB

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K261544Hydro Irrigation SystemEOB · Traditional Stryker Instruments06/17/2026SE
K254133ENTity USB Videoscope SystemEOB · Traditional Optim, LLC05/14/2026SE
K253184Video Rhinolaryngoscope System (Disposable Video Rhinolaryngoscope SP11A Endoscopic…EOB · Traditional Zhuhai Wesee Meditech Co., Ltd.03/25/2026SE
K252050Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241DEOB · Traditional Olympus Medical Systems Corporation03/20/2026SE
K241731Outlook Surgical Versa One System (8900139)EOB · Traditional Resnent, LLC08/11/2025SE
K243639Portare System (FA-001)EOB · Traditional Grumpy Innovation, Inc.06/05/2025SE
K234096MonoStereoEOB · Traditional Medicaltek Co., Ltd.09/19/2024SE
K232435Rhinolaryngoscope systemEOB · Traditional Shenzhen HugeMed Medical Technical Development…04/26/2024SE
K232015ATMOS Scope (507.7000.0); ATMOS Scope Pro (507.7050.0); ATMOS Scope iPrime (507.7060.0)EOB · Traditional Atmos Medizintechnik GmbH & Co. KG08/03/2023SE
K222587PatCom Distal Chip EndoscopeEOB · Traditional H&A Mui Enterprises, Inc.07/28/2023SE

More from H&A Mui Enterprises, Inc.

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 S Video System Center Olympus OTV-S500 (Olympus OTV-S500) cleared by the FDA?

Visera S Video System Center Olympus OTV-S500 (Olympus OTV-S500) (K243380) received a 510(k) decision of Substantially Equivalent on March 3, 2025, 124 days after the submission was received.

What is the product code of K243380?

The FDA product code is EOB – Nasopharyngoscope (Flexible Or Rigid), a Class II (moderate risk) device regulated under 21 CFR 874.4760.