# K190993: Kinepict Medical Imaging Tool version v2.2

- Pathway: 510(k) (Traditional)
- Applicant: Kinepict Health, Ltd.
- Decided: Mar 5, 2020 after 324 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: 5 generations back to K010938 (2001). 5 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K153346: syngo Application Software VD11, Siemens Medical Solutions USA, Inc. (2016) Summary page 5.

## Most influential descendants
- K202056: Kinepict Medical Imaging Tool 4.0 (2021), 0 descendants of its own

## Indications for use
Kinepict Medical Imaging Tool version v2.2 is intended to be used to visualize blood vessel structures by detecting the movement of the contrast medium bolus in standard-of-care angiography examination. This software is intended to be used in addition to, or as replacement for current DSA imaging. Kinepict Software can be deployed on independent hardware such as a stand-alone diagnostic review, post-processing, and reporting workstation. It can also be configured within a network to send and receive DICOM data. Furthermore, Kinepict Software can be deployed on systems of several angiography system family. It provides image guided solutions in the operating room, for image guided surgery, by Image Fusion and by navigation systems, image guided solutions in interventional cardiology and electrophysiology and image guided solutions for interventional oncology, interventional radiology, and interventional neuroradiology. Kinepict Software can also be combined with fluoroscopy systems or Radiographic systems.

Source page: https://510kreport.com/device/K190993
Methodology: https://510kreport.com/methodology