# K192518: Reusable Monopolar Active Cord

- Pathway: 510(k) (Traditional)
- Applicant: Us Endoscopy
- Decided: Oct 25, 2019 after 42 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
Longest line of descent: 1 generation back to K982748 (1998). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K982748: BI-Polar Cord Set 1.88 TR, BI-Polar Cord Set 1.83 TR, Model #'S SB223, SB 224, New Deantronics Taiwan, Ltd. (1998) Summary page 5.

## Indications for use
The Reusable Monopolar Active Cord is intended to deliver monopolar electrical current from the electrosurgical unit to electrosurgical devices or accessories requiring monopolar electrical current during endoscopic procedures.

Source page: https://510kreport.com/device/K192518
Methodology: https://510kreport.com/methodology