# K150102: SnoreSounds

- Pathway: 510(k) (Traditional)
- Applicant: Appian Medical, Inc.
- Decided: Nov 5, 2015 after 289 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
SnorcSounds software is indicated for use as an aid in the diagnostic cvaluation of snoring in paticnts. The software provides quantitative and qualitative analysis of snoring.

Source page: https://510kreport.com/device/K150102
Methodology: https://510kreport.com/methodology