K241620
- 510(k) number
- K241620
- Device name
- ChestView US
- Applicant
- Gleamer Sas FR
- Product code
- MYN — Analyzer, Medical Image
- Decision date
- 2025-02-27
- Date received
- 2024-06-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.1 MB · U.S. public domain
Also available from FDA: K241620.pdf
Official FDA record: K241620
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.