K242992
- 510(k) number
- K242992
- Device name
- RayCare (2024A SP1)
- Applicant
- RaySearch Laboratories AB (PUBL) SE
- Product code
- MUJ — System, Planning, Radiation Therapy Treatment
- Decision date
- 2025-04-17
- Date received
- 2024-09-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K242992.pdf
Official FDA record: K242992
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.