# K982099: Momentum NO. FS008 Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: Sriram Enterprises D.B.A. Momentum Group
- Decided: Oct 5, 1998 after 112 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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
These Manual Wheelchairs are to be used by people needing mobility assistance. The manual Wheelchairs will be used for personal use, and for commercial use in venues such as Theme parks, Airports, and Hospitals.

Source page: https://510kreport.com/device/K982099
Methodology: https://510kreport.com/methodology