# K203293: Abbott Medical Grounding Pad, model RF-DGP-IS

- Pathway: 510(k) (Traditional)
- Applicant: Abbott Medical
- Decided: Jan 21, 2022 after 438 days
- Product code: GXD (Generator, Lesion, Radiofrequency)
- Device class: 2
- Regulation: 21 CFR 882.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K853291 (1985). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K130027: Disposable Neutral Electrode GP202, Cathay Manufacturing Corp. (2013) Summary page 4.

## Indications for use
This disposable electrosurgical return electrode with conductive adhesive gel is used in monopolar electrosurgical procedures for adult patients.

Source page: https://510kreport.com/device/K203293
Methodology: https://510kreport.com/methodology