K240114
- 510(k) number
- K240114
- Device name
- UltraEzAir® (UEA1A)
- Applicant
- Dualams, Inc., Dba Airkor TX · US
- Product code
- CCT — Applicator (Laryngo-Tracheal), Topical Anesthesia
- Decision date
- 2024-10-16
- Date received
- 2024-01-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K240114.pdf
Official FDA record: K240114
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.