K240841
- 510(k) number
- K240841
- Device name
- Digital Radiography System (ManntiX B, ManntiX K)
- Applicant
- Shenzhen Browiner Tech Co., Ltd. CN
- Product code
- IZL — System, X-Ray, Mobile
- Decision date
- 2024-12-09
- Date received
- 2024-03-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K240841.pdf
Official FDA record: K240841
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.