VUZE System— 510(k) K210830

Substantially Equivalent

Vuze Medical , Ltd.

FDA 510(k) clearance K210830 for VUZE System, Substantially Equivalent on 2022-01-03. Applicant: Vuze Medical , Ltd..

Clearance details

Applicant: Vuze Medical , Ltd.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2021-03-19
Decision date: 2022-01-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ra'Anana, IL

Download summary PDF View on FDA.gov ↗

Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

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.