# K002237: P3IMRT TM

- Pathway: 510(k) (Traditional)
- Applicant: Adac Laboratories
- Decided: Feb 2, 2001 after 193 days
- Product code: MUJ (System, Planning, Radiation Therapy Treatment)
- Device class: 2
- Regulation: 21 CFR 892.5050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
73 later devices descend from it; 5 cite it directly.
0 of 74 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
- K032724: PINNACLE3 Radiation Therapy Planning System (2003), 44 descendants of its own
- K041577: PINNACLE3 Radiation Therapy Planning System (2004), 39 descendants of its own
- K080799: Atlas-Based Autosegmentation (2008), 29 descendants of its own
- K013673: HI-Art System (2002), 27 descendants of its own
- K033347: Modification to: HI-Art System (2003), 26 descendants of its own

Source page: https://510kreport.com/device/K002237
Methodology: https://510kreport.com/methodology