# K041782: Seemor 5.0 Image Display Program

- Pathway: 510(k) (Traditional)
- Applicant: Areeda Assoc., Ltd.
- Decided: Aug 16, 2004 after 46 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K992317 (1999). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K992317: Autospect Plus with Instill Motion Correction, Adac Laboratories (1999) Summary page 1.

## Indications for use
SeeMorTM 5.0 software program should be used for the transfer, display and image manipulation of multimodality diagnostic medical images and for the reorientation, and filtered backprojection reconstruction of SPECT & PET gated and ungated myocardial perfusion data.

Source page: https://510kreport.com/device/K041782
Methodology: https://510kreport.com/methodology