510(k) K252109

Device
RayStation (2024A SP3)
Applicant
RaySearch Laboratories AB (PUBL)
510(k) number
K252109
Product code
MUJ
Decision
Substantially Equivalent (SESE)
Decision date
2025-12-22
Date received
2025-07-07
Regulation
892.5050
Classification name
System, Planning, Radiation Therapy Treatment
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Olympiada Lachana
Address
Eugeniavägen 18c Stockholm SE 113 68 113 68

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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