GARAVENTA SUPER-TRAC TRE-52— 510(k) K020933

Name: FDA 510(k) clearance K020933
Creator: U.S. Food and Drug Administration
Published: 2002-04-04

Substantially Equivalent

Garaventa Accessibility

FDA 510(k) clearance K020933 for GARAVENTA SUPER-TRAC TRE-52, Substantially Equivalent on 2002-04-04. Applicant: Garaventa Accessibility. Device class: 2.

Clearance details

Applicant: Garaventa Accessibility
Product code: Code ING
Device class: Class 2
Regulation: 21 CFR 890.3930
Advisory panel: Physical Medicine
Date received: 2002-03-22
Decision date: 2002-04-04
Decision: Substantially Equivalent
Clearance type: Special
Location: Blain, WA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code ING

product code ING

Death: 3
Total: 3

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.