myTAP2— 510(k) K181482

Name: FDA 510(k) clearance K181482
Creator: U.S. Food and Drug Administration
Published: 2018-08-31

Substantially Equivalent

Airway Management, Inc.

FDA 510(k) clearance K181482 for myTAP2, Substantially Equivalent on 2018-08-31. Applicant: Airway Management, Inc.. Device class: 2.

Clearance details

Applicant: Airway Management, Inc.
Product code: Code LRK
Device class: Class 2
Regulation: 21 CFR 872.5570
Advisory panel: Dental
Date received: 2018-06-05
Decision date: 2018-08-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carrollton, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LRK

view all

K262104 — Anti Snoring Mouthpiece (L09-BB, L09-PP, L09-TB, L09-BT, L09-TP, L09-PT, L09-TT)2026-08-27
K261912 — SnØreNegatØr2026-07-31
K261366 — Virtus2026-06-12
K261251 — Snorbliss® Anti-Snoring Device2026-06-11
K261134 — Dormiva Anti-Snoring Mouth Guard2026-05-14

More clearances from Airway Management, Inc.

view all

K160239 — TAP 3, TAP 12016-08-10
K122350 — TAP PAP NASAL PILLOW MASK2012-11-01
K062951 — TAP III ANTI-SNORING DEVICE2006-12-12
K061732 — TAP-T2006-07-12
K060388 — TAP II ANTI-SNORING AND OBSTRUCTIVE SLEEP APNEA ORAL APPLIANCE WITH ATTACHMENT2006-05-17

Adverse events under product code LRK

product code LRK

Injury: 246
Malfunction: 1,044
Total: 1,290

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.