# K082204: Series SY Disposable Electrosurgical Pad

- Pathway: 510(k) (Traditional)
- Applicant: Ventlab Corp.
- Decided: Aug 13, 2008 after 8 days
- Product code: ODR (Electrosurgical Patient Return Electrode)
- 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.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Ventlab Disposable ElectrosurgicalPad is applied to the patient during electrosurgical procedures to provide a path for RF current to leave the patient and return to the generator.

Source page: https://510kreport.com/device/K082204
Methodology: https://510kreport.com/methodology