EZ-LIGHT 4000 SERIES MANUAL WHEELCHAIR— 510(k) K002669

Name: FDA 510(k) clearance K002669
Creator: U.S. Food and Drug Administration
Published: 2000-10-11

Substantially Equivalent

Jiangsu Intco Medical Equipment & Supply Co., Ltd.

FDA 510(k) clearance K002669 for EZ-LIGHT 4000 SERIES MANUAL WHEELCHAIR, Substantially Equivalent on 2000-10-11. Applicant: Jiangsu Intco Medical Equipment & Supply Co., Ltd.. Device class: 1.

Clearance details

Applicant: Jiangsu Intco Medical Equipment & Supply Co., Ltd.
Product code: Code IOR
Device class: Class 1
Regulation: 21 CFR 890.3850
Advisory panel: Physical Medicine
Date received: 2000-08-28
Decision date: 2000-10-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chino, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IOR

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K261075 — Manual Wheelchair (MS01); Manual Wheelchair (MA01)2026-06-22
K261076 — Caregiver-assisted wheelchair (MS02); Caregiver-assisted wheelchair (MA02)2026-06-22
K260849 — ICON 35; ICON 45; ICON 60; ICON 30FAF2026-06-11

More clearances from Jiangsu Intco Medical Equipment & Supply Co., Ltd.

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K002670 — EZ-TRAVELER 3000 SERIES MANUAL WHEELCHAIR2000-10-11
K002671 — EZ-TRAVELER 2500 SERIES MANUAL WHEELCHAIR2000-10-11
K002673 — EZ-COMFORT TRANSPORTER 2000 SERIES2000-10-11

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.