LEVO MAX— 510(k) K140706

Substantially Equivalent

Levo AG

FDA 510(k) clearance K140706 for LEVO MAX, Substantially Equivalent on 2015-01-21. Applicant: Levo AG.

Clearance details

Applicant: Levo AG
Product code: Code ITI
Advisory panel: Physical Medicine
Date received: 2014-03-21
Decision date: 2015-01-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: 5610 Wohlen, CH

Download summary PDF View on FDA.gov ↗

Adverse events under product code ITI

product code ITI

Death: 34
Injury: 778
Malfunction: 1,085
Other: 1
Total: 1,898

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.