# K073450: Sutter Electrosurgical Cables

- Pathway: 510(k) (Traditional)
- Applicant: Sutter Medizintechnik GmbH
- Decided: Mar 17, 2008 after 98 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.
7 later devices descend from it; 4 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K111262: Electrosurgical Monopolar Cable/Adapters, Electrosurgical Bipolar Cable/ Adapters, Bipolar Electrosurgical Cables, Monop (2012), 3 descendants of its own
- K081678: Conmed Beamer System C600 (2008), 1 descendant of its own
- K241621: Da Vinci Monopolar and Bipolar Adapters (378896) (2024), 0 descendants of its own
- K143662: Bissinger Monopolar Forceps and Cables (2015), 0 descendants of its own
- K150024: Bissinger Monopolar Cables (2015), 0 descendants of its own

## Indications for use
To electrically connect monopolar/bipolar electrosurgical instruments to an electrosurgical generator.

Source page: https://510kreport.com/device/K073450
Methodology: https://510kreport.com/methodology