# K071556: Somnoscreen EEG10-20

- Pathway: 510(k) (Special)
- Applicant: Somnomedics GmbH
- Decided: Jul 18, 2007 after 41 days
- Product code: MNR (Ventilatory Effort Recorder)
- Device class: 2
- Regulation: 21 CFR 868.2375
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K000396 (2000). 4 ancestors in all.
5 later devices descend from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060708: Somnoscreen, Somnomedics GmbH & Co. KG (2007) Summary page 2.

## Most influential descendants
- K201054: SOMNOscreen plus (2020), 4 descendants of its own
- K241288: Noxturnal Web (2024), 2 descendants of its own
- K261747: Report Studio (2026), 0 descendants of its own
- K260585: Noxturnal Web (2026), 0 descendants of its own
- K240700: HomeSleepTest (HST, HST REM+) (2024), 0 descendants of its own

## Indications for use
The SOMNOscreen UEGIO20 is a non-life-supporting portable physiological signal recording device intended to be used for testing adult patients suspected of having sleep-related breathing disorders.

Source page: https://510kreport.com/device/K071556
Methodology: https://510kreport.com/methodology