# K972563: Lift Master

- Pathway: 510(k) (Traditional)
- Applicant: Mechanical Application Designs, Inc.
- Decided: Aug 22, 1997 after 44 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
No predicates in its family tree.
3 later devices descend from it; 1 cites 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)
- None. The FDA summary names its predicate without a number.
- (no number) Permobil Chairman System: named in the summary without a submission number

## Most influential descendants
- K992828: E-2000 Power Elevating Seat System, Models Ard-Estorm, Ard-EP320, Ard-Elancer (2000), 2 descendants of its own
- K013516: Invacare Elevating Seat Option ESS6 (2001), 1 descendant of its own
- K033819: Invacare 3G Tarsys (2004), 0 descendants of its own

## Indications for use
THE LIFT MASTER ELEVATING POWER SEAT ASSEMBLY DESIGN IS INTENDED FOR USE ON A POWER AND MANUAL WHEELCHAIR. THE LIFT MASTER WILL ELEVATE PATIENTS TO A GREATER HEIGHT THAN THAT OF THE CONVENTIONAL SEAT HEIGHT OF A WHEELCHAIR.

Source page: https://510kreport.com/device/K972563
Methodology: https://510kreport.com/methodology