# K201575: CMDR 2C (Multiple Models)

- Pathway: 510(k) (Special)
- Applicant: Minxray, Inc.
- Decided: Jul 8, 2020 after 27 days
- Product code: IZL (System, X-Ray, Mobile)
- Device class: 2
- Regulation: 21 CFR 892.1720
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 11 generations back to K896095 (1990). 23 ancestors in all.
No later device cites it as a predicate yet.
0 of 24 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K191451: CMDR 2CW (Multiple models), Minxray, Inc. (2019) Summary page 4.

## Indications for use
Intended for use by a qualified/trained physician or technician on both adult and pediatric subjects for taking diagnostic x-rays. Not for mammography.

Source page: https://510kreport.com/device/K201575
Methodology: https://510kreport.com/methodology