510(k) K242463

ARIA Radiation Therapy Management System (18.1) by Varian Medical Systems, Inc. — Product Code MUJ

K242463 is an FDA 510(k) premarket notification submitted by Varian Medical Systems, Inc. for the device "ARIA Radiation Therapy Management System (18.1)". The FDA issued a decision of Substantially Equivalent on December 13, 2024. The device falls under product code MUJ (System, Planning, Radiation Therapy Treatment), a Class II device regulated under 21 CFR 892.5050. Varian Medical Systems, Inc. has at least 10 other 510(k) clearances on record.