# K123970: Caas Intravascular

- Pathway: 510(k) (Traditional)
- Applicant: Pie Medical Imaging BV
- Decided: Feb 6, 2013 after 42 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: 6 generations back to K941322 (1995). 6 ancestors in all.
1 later device descends from it; 1 cites 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)
- K092842: Echoplaque, Indec Systems, Inc. (2010) Summary page 1.

## Most influential descendants
- K210931: Libby IAAA v1.0 (2021), 0 descendants of its own

## Indications for use
Based on Intravascular ultrasound (IVUS) and/or optical coherence tomography (OCT) images CAAS IntraVascular enables quantification of artery and/or stent dimensions.

Source page: https://510kreport.com/device/K123970
Methodology: https://510kreport.com/methodology