510(k) K181903

BRAVOS Afterloader Family: BRAVOS Afterloader System, Transfer Guide Tubes, and Length Assessment Device by Varian Medical Systems, Inc. — Product Code JAQ

K181903 is an FDA 510(k) premarket notification submitted by Varian Medical Systems, Inc. for the device "BRAVOS Afterloader Family: BRAVOS Afterloader System, Transfer Guide Tubes, and Length Assessment Device". The FDA issued a decision of Substantially Equivalent on Oct 3, 2018. The device falls under product code JAQ (System, Applicator, Radionuclide, Remote-Controlled), a Class II device regulated under 21 CFR 892.5700. Varian Medical Systems, Inc. has 205 other 510(k) clearances on record.