# K240992: eMVFit (MVF-10M)

- Pathway: 510(k) (Traditional)
- Applicant: Weero Co., Ltd.
- Decided: Oct 10, 2024 after 182 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: 25 generations back to K943450 (1995). 344 ancestors in all.
No later device cites it as a predicate yet.
0 of 345 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K210877: Evolve System with the T3 Applicator, InMode, Ltd. (2021) Summary page 6.
- K201285: InMode Evolve System with the Tone Applicator, InMode, Ltd. (2021) Summary page 5.
- K212832: TimeWaver Frequency, Timewaver Production GmbH (2021) Summary page 5.

## Indications for use
EMS is used for: * Relaxation of muscle spasms * Prevention or retardation of disuse atrophy * Increasing local blood circulation * Muscle re-education * Maintaining or increasing range of motion * Immediate postsurgical stimulation of calf muscles to prevent venous thrombosis

Source page: https://510kreport.com/device/K240992
Methodology: https://510kreport.com/methodology