ECHELON Oval V6.2 MRI System— 510(k) K221619

Substantially Equivalent

Fujifilm Healthcare Corporation

FDA 510(k) clearance K221619 for ECHELON Oval V6.2 MRI System, Substantially Equivalent on 2023-01-26. Applicant: Fujifilm Healthcare Corporation.

Clearance details

Applicant: Fujifilm Healthcare Corporation
Product code: Code LNH
Advisory panel: Radiology
Date received: 2022-06-03
Decision date: 2023-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kashiwa-Shi, JP

Download summary PDF View on FDA.gov ↗

Adverse events under product code LNH

product code LNH

Death: 11
Injury: 670
Malfunction: 1,460
Other: 2
Total: 2,143

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.