# K102910: Model Luna Manual Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: P.D.G., Inc.
- Decided: Dec 23, 2010 after 83 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
Longest line of descent: 1 generation back to K002317 (2000). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K002317: Model 9000 Bariatric Wheelchair, Invacare Corp. (2000) Summary page 1.

## Indications for use
To provide mobility to persons limited to a seated position.

Source page: https://510kreport.com/device/K102910
Methodology: https://510kreport.com/methodology