# K960508: Pathway Electromyograph Model Pathway II/MR-10/MR-15/MR-20/MR-25

- Pathway: 510(k) (Traditional)
- Applicant: The Prometheus Group
- Decided: Jan 16, 1997 after 346 days
- Product code: HIR (Perineometer)
- Device class: 2
- Regulation: 21 CFR 884.1425
- 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/K960508
Methodology: https://510kreport.com/methodology