# K182888: MRCAT Pelvis

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems MR Finland
- Decided: Apr 30, 2019 after 197 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
Longest line of descent: 10 generations back to K010975 (2001). 32 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 36 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K151435: MRCAT, Philips Medical Systems MR Finland (2016) Summary page 5.

## Most influential descendants
- K193109: MRCAT brain (2020), 2 descendants of its own
- K211841: MRI Planner (2022), 0 descendants of its own
- K214081: MRCAT Head & Neck (2022), 0 descendants of its own

## Indications for use
MRCAT Pelvis is a software add-on for Ingenia 1.5T and 3.0T MR systems. Intended Use: MRCAT imaging is intended to provide the operator with information of tissue properties for radiation attenuation estimation purposes in photon external beam radiotherapy treatment planning. Indications for use: MRCAT Pelvis is indicated for radiotherapy treatment planning of soft tissue cancers in the pelvic region.

Source page: https://510kreport.com/device/K182888
Methodology: https://510kreport.com/methodology