# K973038: Adjustable Therasnore

- Pathway: 510(k) (Traditional)
- Applicant: Distar, Inc.
- Decided: Nov 12, 1997 after 90 days
- Product code: LRK (Device, Anti-Snoring)
- Device class: 2
- Regulation: 21 CFR 872.5570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 2 cite it directly.
0 of 5 devices 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.

## Most influential descendants
- K062333: Laimad (2006), 2 descendants of its own
- K140663: Therasnore (2014), 0 descendants of its own
- K101155: Auradorm (Neuromuscular Sleep) (2011), 0 descendants of its own
- K101709: Lambergsleepwell- Smartrusion (LSW-S) (2010), 0 descendants of its own

## Indications for use
The Adjustable TheraSnore is a treatment for snoring.

Source page: https://510kreport.com/device/K973038
Methodology: https://510kreport.com/methodology