K242731
- 510(k) number
- K242731
- Device name
- MasteRad MiniX Mobile Digital Imaging System (Mini-X)
- Applicant
- Medicatech USA, Inc. CA · US
- Product code
- OWB — Interventional Fluoroscopic X-Ray System
- Decision date
- 2025-05-16
- Date received
- 2024-09-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.4 MB · U.S. public domain
Also available from FDA: K242731.pdf
Official FDA record: K242731
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.