# K042650: Biomove 3000

- Pathway: 510(k) (Traditional)
- Applicant: Curatronic, Ltd.
- Decided: Jan 27, 2005 after 121 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
Longest line of descent: 1 generation back to K012885 (2001). 2 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K012885: Neuromove NM900, Dan Med, Inc. (2001) Summary page 1.
- K032955: Automove, Model AM800, Danmeter A/S (2003) Summary page 1.

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

## Indications for use
The Biomove 3000 is indicated for: 1. Stroke Rehabilitation by Muscle Re-education 2. Prevention or retardation of disuse atrophy 3. Increasing local blood circulation 4. Muscle re-education 5. Maintaining or increasing range of motion

Source page: https://510kreport.com/device/K042650
Methodology: https://510kreport.com/methodology