K251402
- 510(k) number
- K251402
- Device name
- LIA-1 Catheter (542-1)
- Applicant
- Leadoptik, Inc. CA · US
- Product code
- KTI — Bronchoscope Accessory
- Decision date
- 2025-12-19
- Date received
- 2025-05-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ear, Nose, Throat
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K251402.pdf
Official FDA record: K251402
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.