# K031158: Swift 2.0, Model 132.001

- Pathway: 510(k) (Special)
- Applicant: Nucletron Corp.
- Decided: Aug 7, 2003 after 118 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
Longest line of descent: 3 generations back to K911612 (1991). 4 ancestors in all.
3 later devices descend from it; 2 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K022739: Real Time HDR (220V), Model 132.001; Real Time HDR (110V), Model 132.002, Nucletron Corporation (2002) Summary page 2.

## Most influential descendants
- K112420: Oncentra Prostate 4.0 (2011), 1 descendant of its own
- K170841: BiopSee, Mobile US (2017), 0 descendants of its own
- K080929: Oncentra Gyn (2008), 0 descendants of its own

## Indications for use
Swift is a software application for Brachytherapy Treatment Planning, for the treatment of cancer, i.e. intercavitary, interstitial, intraluminal, involving radioactive sources.

Source page: https://510kreport.com/device/K031158
Methodology: https://510kreport.com/methodology