# K110705: Apnea Risk Evaluation System (Ares)

- Pathway: 510(k) (Special)
- Applicant: Advanced Brain Monitoring, Inc.
- Decided: Apr 14, 2011 after 31 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: 2 generations back to K003154 (2001). 4 ancestors in all.
41 later devices descend from it; 1 cites it directly.
0 of 46 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K071230: Apnea Risk Evaluation System (Ares), Model 600, Advanced Brain Monitoring, Inc. (2007) Summary page 1.

## Most influential descendants
- K111194: Apnea Risk Evaluation System (Ares) (2011), 40 descendants of its own
- K112514: Apnea Risk Evaluation System (Ares) (2012), 38 descendants of its own
- K120447: X4 (2012), 18 descendants of its own
- K130013: X4 System (2013), 17 descendants of its own
- K120450: Sleep Profiler (2012), 16 descendants of its own

## Indications for use
The Apnea Risk Evaluation System (ARES), Model 610 is indicated for use in the diagnostic evaluation by a physician of adult patients with possible sleep apnea. The ARES can record and score respiratory events during sleep (e.g., apneas, hypopneas, mixed apneas and flow limiting events). The device is designed for prescription use in home diagnosis of adults with possible sleep-related breathing disorders.

Source page: https://510kreport.com/device/K110705
Methodology: https://510kreport.com/methodology