Clearance Summary
LifeVac received FDA 510(k) clearance under submission number DEN250012, sponsored by Lifevac, LLC. The device was reviewed via the Direct premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2026-03-04.
- Submission: DEN250012
- Applicant / Sponsor: Lifevac, LLC
- Clearance pathway: Direct
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.5400
- Decision date: 2026-03-04
Classification & Regulation
This clearance is catalogued under FDA product code QXN and 21 CFR 874.5400, within the Ear, Nose, Throat review panel as a Class II device.