# K952913: Applicators for Varian Varisource Remote High Soes Rate Afterloader

- Pathway: 510(k) (Traditional)
- Applicant: Varian Assoc., Inc.
- Decided: Nov 22, 1995 after 149 days
- Product code: JAQ (System, Applicator, Radionuclide, Remote-Controlled)
- Device class: 2
- Regulation: 21 CFR 892.5700
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
18 later devices descend from it; 6 cite it directly.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K113766: Clickfit Transfer Guide Tubes Needle Clickfit Transfer Guide Tubes Catheter Transfer Guide Tube Set Varisource Luer Tran (2012), 5 descendants of its own
- K955844: Applicators for Varian Varisource Remote High Dose Rate Afterloader (1996), 4 descendants of its own
- K141336: Source Guide Tube with Locking Mechanism for 113 MM Needles, Gammamedplus (2014), 3 descendants of its own
- K073133: Interstitial Needles (2007), 3 descendants of its own
- K181903: BRAVOS Afterloader Family: BRAVOS Afterloader System, Transfer Guide Tubes, and Length Assessment Device (2018), 2 descendants of its own

Source page: https://510kreport.com/device/K952913
Methodology: https://510kreport.com/methodology
