# K063560: Hilger Dual-Stim Nerve Stimulator

- Pathway: 510(k) (Abbreviated)
- Applicant: Wr Medical Electronics Co.
- Decided: Jan 5, 2007 after 38 days
- Product code: ETN (Stimulator, Nerve)
- Device class: 2
- Regulation: 21 CFR 874.1820
- 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 K895838 (1990). 2 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K895838: Brackmann Emg Monitoring System, Wr Medical Electronics Co. (1990) Summary page 1.
- K021595: Gyrus Ent Nerve Stimulator, Gyrus Ent LLC (2002) Summary page 1.
- (no number) Hilger Facial Nerve Stimulator: named in the summary without a submission number

## Most influential descendants
- K081742: Baxano Neural Localization Probe 1.75 and 1.25 (2008), 2 descendants of its own
- K092729: Baxano Neuro Check Device (2009), 1 descendant of its own
- K110696: Neuro Check Device with IO-Flex Wire (2011), 0 descendants of its own

## Indications for use
The Hilger Dual-Stim Nerve Stimulator provides electrical stimulation to nerves during diagnostic and surgical procedures.

Source page: https://510kreport.com/device/K063560
Methodology: https://510kreport.com/methodology