# K061417: Genicon Disposable Electrosurgical Instrumentation, Model 533-005-910

- Pathway: 510(k) (Traditional)
- Applicant: Genicon
- Decided: Oct 10, 2006 after 141 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: 2 generations back to K910831 (1991). 2 ancestors in all.
6 later devices descend from it; 3 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K984240: Endopath Endoscopic Instruments, Ethicon Endo-Surgery, Inc. (1999) Summary page 1.

## Most influential descendants
- K132771: Kingston Endoscopic Surgical Instruments (2014), 2 descendants of its own
- K171825: Disposable Endoscopic Surgical Instrument, Reusable Endoscopic Surgical Instrument (2018), 1 descendant of its own
- K171752: X-Surge (2017), 1 descendant of its own
- K211019: Disposable Monopolar Laparoscopic Tips and Reusable Handles (2021), 0 descendants of its own
- K210569: Disposable Monopolar Laparoscopic Shafts and Reusable Handles (2021), 0 descendants of its own

## Indications for use
Endoscopic surgical procedures. It is a family of instruments which includes graspers, dissectors, and scissors, which are intended to be used to grasp, manipulate, cut, and cauterize soft tissue.

Source page: https://510kreport.com/device/K061417
Methodology: https://510kreport.com/methodology