Evis Exera III Duodenovideoscope Olympus TJF-Q190V— 510(k) K202661

Substantially Equivalent

Olympus Medical Systems Corp.

FDA 510(k) clearance K202661 for Evis Exera III Duodenovideoscope Olympus TJF-Q190V, Substantially Equivalent on 2020-12-08. Applicant: Olympus Medical Systems Corp..

Clearance details

Applicant: Olympus Medical Systems Corp.
Product code: Code FDT
Advisory panel: Gastroenterology, Urology
Date received: 2020-09-14
Decision date: 2020-12-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hachioji-Shi, JP

Download summary PDF View on FDA.gov ↗

Adverse events under product code FDT

product code FDT

Death: 86
Injury: 1,954
Malfunction: 14,912
Total: 16,952

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.