# K062241: Adjustable Multi-Catheter Source Applictor

- Pathway: 510(k) (Traditional)
- Applicant: North American Scientific, Inc.
- Decided: Nov 9, 2006 after 99 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.
15 later devices descend from it; 1 cites it directly.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K071229: Senorad Multi-Lumen Balloon Source Applicator for Branchytherapy (2007), 14 descendants of its own
- K081079: Contura MLB Source Applicator for Brachytherapy (2008), 11 descendants of its own
- K091378: Mammosite II Radiation Therapy System (2009), 9 descendants of its own
- K121653: Intrabeam System with Intrabeam Spherical Applicators (2012), 8 descendants of its own
- K133655: Radiance V2 (2014), 5 descendants of its own

## Indications for use
The Adjustable Multi-Catheter Source Applicator is intended to provide brachytherapy when the physician chooses to deliver intracavitary radiation to the surgical margins following lumpectomy of breast cancer.

Source page: https://510kreport.com/device/K062241
Methodology: https://510kreport.com/methodology