# K080787: Biomove 5000 System

- Pathway: 510(k) (Special)
- Applicant: Curatronic, Ltd.
- Decided: Apr 17, 2008 after 28 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: 2 generations back to K012885 (2001). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K042650: Biomove 3000, Curatronic, Ltd. (2005) Summary page 2.

## Indications for use
The Biomove 5000 is indicated for: 1. Stroke Rehabilitation by Muscle Re-education 2. Prevention of 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/K080787
Methodology: https://510kreport.com/methodology