# K954334: Acuplus

- Pathway: 510(k) (Traditional)
- Applicant: S.H.P. Intl. Pty., Ltd.
- Decided: Jan 22, 1996 after 126 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.
14 later devices descend from it; 1 cites it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K014273: Acustim (2002), 13 descendants of its own
- K051197: Aculife, Model SMW-01 (2006), 9 descendants of its own
- K081943: Model ES-130 (2008), 7 descendants of its own
- K130768: Jiajian CMN Stimulator (2013), 3 descendants of its own
- K202861: Needle Stimulator (2021), 2 descendants of its own

Source page: https://510kreport.com/device/K954334
Methodology: https://510kreport.com/methodology