# K032955: Automove, Model AM800

- Pathway: 510(k) (Abbreviated)
- Applicant: Danmeter A/S
- Decided: Dec 15, 2003 after 84 days
- Product code: IPF (Stimulator, Muscle, Powered)
- Device class: 2
- Regulation: 21 CFR 890.5850
- 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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K042650: Biomove 3000 (2005), 2 descendants of its own
- K080787: Biomove 5000 System (2008), 0 descendants of its own
- K062631: Myomo E100 (2007), 0 descendants of its own

## Indications for use
Stroke Rehab by Muscle Reeducation Relaxation of muscle spasms Prevention or retardation of disuse atrophy Increasing local blood circulation Muscle re-education Maintaining or increasing range of motion

Source page: https://510kreport.com/device/K032955
Methodology: https://510kreport.com/methodology