# K960673: OSAP

- Pathway: 510(k) (Traditional)
- Applicant: Snorefree, Inc.
- Decided: May 9, 1996 after 79 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
No predicates in its family tree.
102 later devices descend from it; 3 cite it directly.
0 of 103 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
- K972061: TOA (1997), 95 descendants of its own
- K022891: The Breathe EZ Anti-Snoring Device (2003), 75 descendants of its own
- K030440: Oasys-Oral Airway System (2003), 65 descendants of its own
- K060388: Tap II Anti-Snoring and Obstructive Sleep Apnea Oral Appliance with Attachment (2006), 51 descendants of its own
- K061732: TAP-T (2006), 32 descendants of its own

Source page: https://510kreport.com/device/K960673
Methodology: https://510kreport.com/methodology