# K082722: P & F Power Wheelchair, Model HC-500SB

- Pathway: 510(k) (Traditional)
- Applicant: P & F Brother Ind., Corp.
- Decided: Oct 28, 2008 after 41 days
- Product code: ITI (Wheelchair, Powered)
- Device class: 2
- Regulation: 21 CFR 890.3860
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K022697 (2003). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070350: P&F Power Wheelchair, HC-510, P & F Brother Ind., Corp. (2007)

## Indications for use
The device is intended for medical purposes to provide mobility to persons restricted to a sitting position.

Source page: https://510kreport.com/device/K082722
Methodology: https://510kreport.com/methodology