LifeVac— 510(k) DEN250012
UnknownLifevac, LLC
FDA 510(k) clearance DEN250012 for LifeVac, Unknown on 2026-03-04. Applicant: Lifevac, LLC. Device class: 2.
Clearance details
- Applicant
- Lifevac, LLC
- Product code
- Code QXN
- Device class
- Class 2
- Regulation
- 21 CFR 874.5400
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Nesconset, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.