# K960969: Galva 5-T

- Pathway: 510(k) (Traditional)
- Applicant: Zimmer Elektromedizin GmbH
- Decided: May 15, 1996 after 65 days
- Product code: GZJ (Stimulator, Nerve, Transcutaneous, For Pain Relief)
- Device class: 2
- Regulation: 21 CFR 882.5890
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K070888: Combi 8 Max (2008), 2 descendants of its own
- K123642: Muscle Stimulation System (2013), 1 descendant of its own
- K150742: Muscle Stimulation System 110 (2015), 0 descendants of its own

Source page: https://510kreport.com/device/K960969
Methodology: https://510kreport.com/methodology