K242324
- 510(k) number
- K242324
- Device name
- DUTAU-NOVATECH®
- Applicant
- Novatech SA FR
- Product code
- EOQ — Bronchoscope (Flexible Or Rigid)
- Decision date
- 2025-02-06
- Date received
- 2024-08-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ear, Nose, Throat
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K242324.pdf
Official FDA record: K242324
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.