K243473
- 510(k) number
- K243473
- Device name
- PRORAD ATLAS ULTRAPORTABLE; PRORAD ATLAS ULTRAPORTABLE PLUS
- Applicant
- Prognosys Medical Systems Private Limited IN
- Product code
- IZL — System, X-Ray, Mobile
- Decision date
- 2025-07-29
- Date received
- 2024-11-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K243473.pdf
Official FDA record: K243473
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.