Atlas FDA

RayStation

FDA 510(k) clearance K190387 · decided 2019-06-19

Clearance details

K-number
K190387
Device name
RayStation
Applicant
RaySearch Laboratories AB (PUBL)
Decision
Substantially Equivalent
Date received
2019-02-19
Decision date
2019-06-19
Days to decision
120 days
Clearance type
Traditional
Product code
MUJ
Device class
2
Regulation number
892.5050
Medical specialty
Radiology
Advisory committee
Radiology
Location
Stockholm, SE
Third-party review
No
Expedited review
No

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Recalls involving this device

RecordFirmDate
RayStation with the following product descriptions: 1. RayStation 8B, Software Version: 8. recall (Z-2488-2025)RAYSEARCH LABORATORIES AB2025-09-02
Brand Name: RayStation -Intended as a Radiation Therapy Treatment Planning System Model/Ca recall (Z-1186-2025)RAYSEARCH LABORATORIES AB2025-02-19
RayStation 8.1.0.47, 8.1.1.8 and 8.1.2.5. Radiation Therapy Treatment Planning System. recall (Z-1743-2024)RAYSEARCH LABORATORIES AB2024-05-01
RayStation 9.0.0.113 and 9.0.1.142. Radiation Therapy Treatment Planning System. recall (Z-1744-2024)RAYSEARCH LABORATORIES AB2024-05-01
RayStation Software Version Numbers version numbers 8B, 9A, 9B, 10A, 10B, 11A, 11B, 12A, 1 recall (Z-1482-2024)RAYSEARCH LABORATORIES AB2024-04-05
Raystation treatment planning system for radiation therapy, Model Numbers 9.0.0, 9.0.1, 9. recall (Z-1281-2023)RAYSEARCH LABORATORIES AB2023-03-22
RayStation stand-alone software treatment planning system. Models 4.0, 4.3, 4.5, 4.7, 4.9, recall (Z-0866-2020)RAYSEARCH LABORATORIES AB2020-01-27