510(k) Report

FDA applicant

Rolcontrol Products, Co., Inc.

Camarillo, CA10 decisions1988–19880 recalls

FDA records 10 decisions for Rolcontrol Products, Co., Inc. (Camarillo, CA) in 1988: 10 510(k) clearances. Most are in product codes ITI (Wheelchair, Powered) and KNN (Components, Wheelchair). 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 Rolcontrol Products, Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rolcontrol Products, Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Rolcontrol Products, 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