HANDI-LIFT/VICTORY WHEELCHAIR LIFT— 510(k) K893490

Name: FDA 510(k) clearance K893490
Creator: U.S. Food and Drug Administration
Published: 1989-06-12

Substantially Equivalent

The Cheney Co.

FDA 510(k) clearance K893490 for HANDI-LIFT/VICTORY WHEELCHAIR LIFT, Substantially Equivalent on 1989-06-12. Applicant: The Cheney Co.. Device class: 2.

Clearance details

Applicant: The Cheney Co.
Product code: Code ING
Device class: Class 2
Regulation: 21 CFR 890.3930
Advisory panel: Physical Medicine
Date received: 1989-05-04
Decision date: 1989-06-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Berlin, WI, US

Download summary PDF View on FDA.gov ↗

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More clearances from The Cheney Co.

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K896628 — LIBERTY SPECIAL AND LIBERTY STAIRLIFTS1990-01-12
K897019 — HANDI PORCH ELEVATOR1990-01-12
K893544 — HANDI PORCH ELEVATOR & LIBERTY WHEELCHAIR LIFT1989-06-12

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.