Monaco RTP System (6.3)

FDA 510(k) K252002 · Elekta Solutions AB

Substantially Equivalent

510(k) numberK252002

Submission

Device name
Monaco RTP System (6.3)
Applicant
Elekta Solutions AB
Stockholm, SE
Received
June 27, 2025
Decision date
February 19, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MUJ – System, Planning, Radiation Therapy Treatment
Device class
Class II (moderate risk)
Regulation
21 CFR 892.5050
Specialty
Radiology

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Questions and answers

When was Monaco RTP System (6.3) cleared by the FDA?

Monaco RTP System (6.3) (K252002) received a 510(k) decision of Substantially Equivalent on February 19, 2026, 237 days after the submission was received.

What is the product code of K252002?

The FDA product code is MUJ – System, Planning, Radiation Therapy Treatment, a Class II (moderate risk) device regulated under 21 CFR 892.5050.