# K091874: Inomed Adhesive Laryngeal Electrodes, Models 530655, 530656

- Pathway: 510(k) (Traditional)
- Applicant: Inomed Medizintechnik GmbH
- Decided: Nov 18, 2009 after 148 days
- Product code: ETN (Stimulator, Nerve)
- Device class: 2
- Regulation: 21 CFR 874.1820
- 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 K925640 (1993). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
1 of 5 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K071349: Neurosign Laryngeal Electrodes, The Magstim Company, Ltd. (2007) Summary page 1.
- K003745: Laryngeal Surface Electrode-Endotracheal Tube, M-500-ET, Lse-ET, Rln Systems, Inc. (2001) Summary page 1.

## Most influential descendants
- K232888: Disposable Laryngeal Electrodes (2023), 0 descendants of its own

## Indications for use
The Inomed Adhesive Laryngeal Electrodes are intended to be used as a disposable, self-adhesive electrode attached to an endotracheal tube and positioned for continuous EMG monitoring of the larynx during surgical procedures.

Source page: https://510kreport.com/device/K091874
Methodology: https://510kreport.com/methodology