BIOTECH MANUAL WHEELCHAIR B900 SUPER LIGHT WHEELCHAIR— 510(k) K020472

Name: FDA 510(k) clearance K020472
Creator: U.S. Food and Drug Administration
Published: 2002-03-08

Substantially Equivalent

Taiwan Armada Enterprise Co., Ltd.

FDA 510(k) clearance K020472 for BIOTECH MANUAL WHEELCHAIR B900 SUPER LIGHT WHEELCHAIR, Substantially Equivalent on 2002-03-08. Applicant: Taiwan Armada Enterprise Co., Ltd.. Device class: 1.

Clearance details

Applicant: Taiwan Armada Enterprise Co., Ltd.
Product code: Code IOR
Device class: Class 1
Regulation: 21 CFR 890.3850
Advisory panel: Physical Medicine
Date received: 2002-02-12
Decision date: 2002-03-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hsin-Chu City, TW

Download summary PDF View on FDA.gov ↗

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Adverse events under product code IOR

product code IOR

Death: 10
Injury: 232
Other: 2
Total: 244

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.