# K032511: Intuition Image

- Pathway: 510(k) (Traditional)
- Applicant: Brainlab AG
- Decided: Jan 21, 2004 after 160 days
- Product code: LHN (System, Radiation Therapy, Charged-Particle, Medical)
- 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: 2 generations back to K920879 (1992). 8 ancestors in all.
35 later devices descend from it; 2 cite it directly.
0 of 44 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K020631: IPLAN, Brainlab AG (2002) Summary page 1.
- K994413: Brainscan, Brainlab AG (2000) Summary page 1.

## Most influential descendants
- K052220: Iplan RT Fibertracking (2005), 34 descendants of its own
- K080886: Iplan RT Image (2008), 33 descendants of its own
- K103246: Iplan RT (2011), 32 descendants of its own
- K120387: Raystation (2012), 22 descendants of its own
- K130617: Raystation (2013), 21 descendants of its own

## Indications for use
Intuition Image's indications for use is to prepare and present patient and image data based on CT, MR, Angiographic and other imaging sources including - image preparation - image localization - image fusion - image segmentation - isocenter handling - plan review and approval where the result is used for stereotactic radiation treatment planning that is intended for use in stereotactic, conformal, computer planned, LINAC based radiation treatment of cranial, head and neck and extracranial lesions.

Source page: https://510kreport.com/device/K032511
Methodology: https://510kreport.com/methodology