# K926382: Therasnore

- Pathway: 510(k) (Traditional)
- Applicant: Dr. Thomas E. Meade
- Decided: Jul 8, 1993 after 198 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.
154 later devices descend from it; 4 cite it directly.
0 of 155 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K962516: Tap Anti-Snoring Device (1996), 152 descendants of its own
- K042161: Anti-Snoring/Sleep Apnea Device (2004), 109 descendants of its own
- K972061: TOA (1997), 95 descendants of its own
- K050592: Somnomed Mas Rxa (2005), 86 descendants of its own
- K022891: The Breathe EZ Anti-Snoring Device (2003), 75 descendants of its own

Source page: https://510kreport.com/device/K926382
Methodology: https://510kreport.com/methodology