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VISERA S VIDEO SYSTEM CENTER OLYMPUS OTV-S500 (OLYMPUS OTV-S500)

K243380 Class II Traditional
Decision Date
2025-03-03
Sponsor / Applicant
Olympus Medical Systems Corporation

Technical Specification

510(k) Submission ID K243380
Product Code EOB
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4760
Decision Date 2025-03-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VISERA S VIDEO SYSTEM CENTER OLYMPUS OTV-S500 (OLYMPUS OTV-S500) received FDA 510(k) clearance under submission number K243380, sponsored by Olympus Medical Systems Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2025-03-03.

Classification & Regulation

This clearance is catalogued under FDA product code EOB and 21 CFR 874.4760, within the Ear, Nose, Throat review panel as a Class II device.