510(k) Report

FDA applicant

The National Wheel-O-Vator Co., Inc.

Roanoke, IL1 decision1994–19940 recalls

FDA records 1 decision for The National Wheel-O-Vator Co., Inc. (Roanoke, IL) in 1994: 1 510(k) clearance. All are in product code ING (Elevator, Wheelchair, Portable). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, physical medicine panel, where it files most

How often FDA has decided The National Wheel-O-Vator Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The National Wheel-O-Vator Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — The National Wheel-O-Vator Co., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like The National Wheel-O-Vator Co., Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • INGElevator, Wheelchair, Portable1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K934553Wheel-O-VatorThe National Wheel-O-Vator Co., Inc. · 19941cites it

What has FDA decided for it lately?

  • K934553Wheel-O-VatorThe National Wheel-O-Vator Co., Inc. · 1994

The one decision as The National Wheel-O-Vator Co., Inc. →