# K942986: Electrodes (Blade, Ball, Needle, and Loop)

- Pathway: 510(k) (Traditional)
- Applicant: Aaron Medical Industries
- Decided: Mar 21, 1995 after 293 days
- Product code: HGI (Electrocautery, Gynecologic (And Accessories))
- Device class: 2
- Regulation: 21 CFR 884.4120
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 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)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K014201: Aaron Reusable Electrosurgical Electrode (2002), 4 descendants of its own
- K161378: joimax Electrosurgical Instruments (2016), 1 descendant of its own
- K051956: DR. Oppel ST-501 (2005), 1 descendant of its own
- K211173: maxmorespine Bipolar Electrodes (2022), 0 descendants of its own
- K134036: Wavetronic 5000 Digital HF Surgical Unit (2015), 0 descendants of its own

Source page: https://510kreport.com/device/K942986
Methodology: https://510kreport.com/methodology