meddevicedb.com FDA Device Reference

LibAirty Airway Clearance System

K242063 Class II Traditional
Decision Date
2024-12-19
Sponsor / Applicant
Synchrony Medical , Ltd.

Technical Specification

510(k) Submission ID K242063
Product Code BYI
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5665
Decision Date 2024-12-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LibAirty Airway Clearance System received FDA 510(k) clearance under submission number K242063, sponsored by Synchrony Medical , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2024-12-19.

Classification & Regulation

This clearance is catalogued under FDA product code BYI and 21 CFR 868.5665, within the Anesthesiology review panel as a Class II device.