# K152571: Stivax

- Pathway: 510(k) (Traditional)
- Applicant: Biegler GmbH
- Decided: May 26, 2016 after 260 days
- Product code: BWK (Stimulator, Electro-Acupuncture)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K140788 (2014). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K140788: P-STIM, Biegler GmbH (2014) Summary page 4.

## Indications for use
Stivax is an electro-acupuncture device for use in the practice of acupuncture by qualified practitioners of acupuncture as determined by the states.

Source page: https://510kreport.com/device/K152571
Methodology: https://510kreport.com/methodology