# K011993: Quantum Blast

- Pathway: 510(k) (Special)
- Applicant: Pride Mobility Products Corp.
- Decided: Jul 13, 2001 after 17 days
- Product code: ITI (Wheelchair, Powered)
- Device class: 2
- Regulation: 21 CFR 890.3860
- Recalls of this device: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K945936 (1996). 1 ancestor in all.
2 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K945936: JAZZY, Pride Health Care, Inc. (1996) Summary page 1.

## Most influential descendants
- K052353: Z-Chair (2005), 0 descendants of its own
- K032765: Street (2004), 0 descendants of its own

## Recalls of this device
- Jun 25, 2026 · Class II · Z-2844-2026: If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perf
- Jun 25, 2026 · Class II · Z-2853-2026: If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perf
- Apr 11, 2008 · Not classified · Z-1776-2008: Software - Watch dog timer feature was disabled.

## Indications for use
The intended use of the Quantum Blast is to provide mobility for persons limited to a seated position that are capable of operating a powered wheelchair.

Source page: https://510kreport.com/device/K011993
Methodology: https://510kreport.com/methodology