# K173187: MobileDiagnost M50

- Pathway: 510(k) (Traditional)
- Applicant: Philips India Limited
- Decided: Nov 16, 2017 after 45 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: 8 generations back to K981556 (1998). 16 ancestors in all.
No later device cites it as a predicate yet.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K141895: Mobilediagnost WDR, Sedecal., Sa. (2014) Summary page 5.

## Indications for use
The MobileDiagnost M50 is a mobile radiographic system used for general X-ray imaging. This system can be used for taking x-ray images of patients who can’t be moved to a fixed system. Applications include examinations of chest, upper and lower extremities, spinal column, skull radiography and abdominal cavities. MobileDiagnost M50 is not suitable for Mammography.

Source page: https://510kreport.com/device/K173187
Methodology: https://510kreport.com/methodology