# K964028: Sys Stim 226

- Pathway: 510(k) (Traditional)
- Applicant: Mettler Electronics Corp.
- Decided: Feb 3, 1997 after 119 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
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K993229: Analgesic Pulser, Model AP-439 (2001), 1 descendant of its own
- K024036: Product Line-Combo Stimulator/Sequential Stimulator, Model IF-5000 (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K964028
Methodology: https://510kreport.com/methodology