# K183485: CryoVizion System

- Pathway: 510(k) (Traditional)
- Applicant: Cryos Technologies, Inc.
- Decided: Aug 28, 2019 after 254 days
- Product code: LDK (Device, Sensing, Optical Contour)
- Device class: U
- 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 K923792 (1994). 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)
- K923792: Quantec Spinal Measuement System, Quantec Image Processing, Ltd. (1994) Summary page 4.

## Indications for use
The CryoVizion is indicated as a tool to quantify angles on digital photograph depictions such as body angles related to postural asymmetries. It is intended for use in professional health care facilities by health specialists such as podiatrists, orthopedist, physiotherapists, chiropractors, osteopaths, and kinesiotherapists

Source page: https://510kreport.com/device/K183485
Methodology: https://510kreport.com/methodology