Skip to content

Base Only, Toronto Chair

by Intl. Medical Equipment Corp.

510(k) K832322

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 6 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 6 Oct 2026. What this means

Regulatory status

as of registry sync 6 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK832322 Date12 Aug 1983ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 6 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
IQC
Device Class
Class II
Regulation
21 CFR Part 890.3880
Advisory Committee
Physical Medicine
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 6 Oct 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

This device is a wheelchair, special grade, as defined by its classification name and product code IQC. It is a base-only configuration of the Toronto Chair model.

It is supplied as a reusable device, with FDA 510(k) clearance K832322 granted on August 12, 1983, under regulation number 890.3880 for use in physical medicine settings. The device is classified as class II and was cleared via a traditional 510(k) pathway.

Other devices from Intl. Medical Equipment Corp.

Questions

AI-generated answers, 6 Oct 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What is the BASE ONLY, TORONTO CHAIR device used for?

    The BASE ONLY, TORONTO CHAIR is a wheelchair, special grade, designed for use in physical medicine settings. It serves as the base-only configuration of the Toronto Chair model, providing foundational mobility support as defined by its classification under product code IQC and regulation number 890.3880.

  • Is the BASE ONLY, TORONTO CHAIR supplied as a single-use or reusable device?

    The BASE ONLY, TORONTO CHAIR is supplied as a reusable device. This is explicitly stated in the device description, indicating it is intended for multiple uses after appropriate cleaning and maintenance, consistent with its classification as a Class II wheelchair, special grade.

  • What regulatory pathway and clearance number apply to the BASE ONLY, TORONTO CHAIR?

    The BASE ONLY, TORONTO CHAIR received FDA 510(k) clearance K832322 through a traditional 510(k) pathway on August 12, 1983. It was found substantially equivalent (SESE) to a predicate device and is classified as Class II under regulation number 890.3880 for use in physical medicine settings.