# K935853: Emg Trainer

- Pathway: 510(k) (Traditional)
- Applicant: Unitech
- Decided: Jan 18, 1995 after 406 days
- Product code: HCC (Device, Biofeedback)
- Device class: 2
- Regulation: 21 CFR 882.5050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K011823: Biorehab System (2001), 0 descendants of its own

Source page: https://510kreport.com/device/K935853
Methodology: https://510kreport.com/methodology