# K112766: Snorkel

- Pathway: 510(k) (Traditional)
- Applicant: Fellmar Company
- Decided: Jun 4, 2012 after 256 days
- Product code: LQZ (Device, Jaw Repositioning)
- 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
Longest line of descent: 1 generation back to K955503 (1996). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K955503: Adjustable PM Positioner, Jonathan A. Parker, D.D.S. (1996) Summary page 1.

## Indications for use
The Snorkel is used to reduce tongue induced airway obstructions. The Snorkel is intended for use in patients, for the treatment of mild to moderate obstructive sleep apnea.

Source page: https://510kreport.com/device/K112766
Methodology: https://510kreport.com/methodology