# K061732: TAP-T

- Pathway: 510(k) (Special)
- Applicant: Airway Management, Inc.
- Decided: Jul 12, 2006 after 22 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
Longest line of descent: 6 generations back to K882303 (1989). 10 ancestors in all.
32 later devices descend from it; 3 cite it directly.
0 of 43 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K962516: Tap Anti-Snoring Device, Nellcor Puritan Bennett, Inc. (1996) Summary page 1.
- K972061: TOA, W. Keith Thornton, D.D.S. (1997) Summary page 1.
- K060388: Tap II Anti-Snoring and Obstructive Sleep Apnea Oral Appliance with Attachment, Airway Management, Inc. (2006) Summary page 1.

## Most influential descendants
- K103076: Dynaflex (2011), 29 descendants of its own
- K130130: Atg/SM-Osa Appliances (2013), 17 descendants of its own
- K160234: OVENT (2016), 8 descendants of its own
- K161832: O2VENT T (2016), 7 descendants of its own
- K192581: The NightBlocks Appliance (2020), 6 descendants of its own

## Indications for use
To reduce or alleviate night time snoring and mild to moderate obstructive sleep apnea (OSA).

Source page: https://510kreport.com/device/K061732
Methodology: https://510kreport.com/methodology