FDA applicant

Berkeley Electric Wheelchair Co.

Mchenry, IL6 decisions1983–19830 recalls

FDA records 6 decisions for Berkeley Electric Wheelchair Co. (Mchenry, IL) in 1983: 6 510(k) clearances. Most are in product codes KNN (Components, Wheelchair) and ITI (Wheelchair, Powered). 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 Berkeley Electric Wheelchair Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Berkeley Electric Wheelchair Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Berkeley Electric Wheelchair Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Berkeley Electric Wheelchair Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Berkeley”

FDA records each applicant name separately; these may or may not be the same firm.

Berkeley Advanced Biomaterials, Inc. 16 Berkeley Medevices 5 Berkeley Bio-Engineering 4 Berkeley Bio-Medical, Inc. 2

Berkeley Electric Wheelchair Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Berkeley”