# K150024: Bissinger Monopolar Cables

- Pathway: 510(k) (Traditional)
- Applicant: Guenter Bissinger Medizintechnik GmbH
- Decided: Feb 20, 2015 after 44 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 K051610 (2005). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051610: Hans Hermann Laparoscopes and Accessories, Hans Hermann GmbH (2005) Summary page 5.
- K073450: Sutter Electrosurgical Cables, Sutter Medizintechnik GmbH (2008) Summary page 5.

## Indications for use
Cables for electrosurgery are designed to conduct electrical power from the output of a high-frequency electrosurgical generator to the electrosurgical instrument. Do not exceed a maximum output of 6250 Vp of your generator.

Source page: https://510kreport.com/device/K150024
Methodology: https://510kreport.com/methodology