# K011752: Govan+ Wheelchair and Docking Accessory

- Pathway: 510(k) (Traditional)
- Applicant: Accufast, Inc.
- Decided: Jun 28, 2001 after 22 days
- Product code: IOR (Wheelchair, Mechanical)
- Device class: 1
- Regulation: 21 CFR 890.3850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Tracer EX: named in the summary without a submission number

## Indications for use
Therapeutic effect: 1) Provision of out-of-bed seating for disabled persons. 2) Transportation of disabled persons from one location to another in a room or in a building or outdoors. 3) Transportation of disabled persons in the device in motor vehicles. Medical conditions for which the device is indicated: 1) Post-operative weakness or debility. 2) Age-related weakness or debility. 3) Paralysis due to stroke, tumour, etc. 4) Impairment of function due to MS, ALS, Polio. 5) Impairment from physical trauma. 6) Impairment from accidents at birth.

Source page: https://510kreport.com/device/K011752
Methodology: https://510kreport.com/methodology