# K002002: Surefit Dispersive Electrode

- Pathway: 510(k) (Traditional)
- Applicant: Conmedcorp
- Decided: Aug 17, 2000 after 48 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- 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; 2 cite 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
- K102372: Obs Disposable Electrosurgical Pads, Monopolar, Biopolar, Models GBS-DM, GBS-DB (2010), 2 descendants of its own
- K130027: Disposable Neutral Electrode GP202 (2013), 1 descendant of its own
- K100047: Surefit Dual Dispersive Electrode (2010), 1 descendant of its own
- K203293: Abbott Medical Grounding Pad, model RF-DGP-IS (2022), 0 descendants of its own
- K120322: Conmed Surefit Dual Dispersive Electrode (2012), 0 descendants of its own

Source page: https://510kreport.com/device/K002002
Methodology: https://510kreport.com/methodology