THE LIBERATOR WHEELCHAIR— 510(k) K010859

Substantially Equivalent

Liberator Wheelchairs, Inc.

FDA 510(k) clearance K010859 for THE LIBERATOR WHEELCHAIR, Substantially Equivalent on 2001-04-05. Applicant: Liberator Wheelchairs, Inc..

Clearance details

Applicant: Liberator Wheelchairs, Inc.
Product code: Code ITI
Advisory panel: Physical Medicine
Date received: 2001-03-22
Decision date: 2001-04-05
Decision: Substantially Equivalent
Clearance type: Special
Location: Halton City, TX, US

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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.