# K151419: GF50A

- Pathway: 510(k) (Traditional)
- Applicant: Samsung Electronics Co., Ltd.
- Decided: Jun 23, 2015 after 26 days
- Product code: KPR (System, X-Ray, Stationary)
- Device class: 2
- Regulation: 21 CFR 892.1680
- 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 K862120 (1986). 7 ancestors in all.
19 later devices descend from it; 1 cites it directly.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K140326: Xgeo GF50, Samsung Electronics Co., Ltd. (2014) Summary page 4.

## Most influential descendants
- K180543: GC70, GU60A&GU60A-65, GF50, GF50A, GR40CW, and GM85 (2018), 18 descendants of its own
- K181626: Digital Diagnostic Mobile X-ray System (2018), 10 descendants of its own
- K181631: GR40CW (2018), 5 descendants of its own
- K183292: Topaz Mobile DR System (2019), 4 descendants of its own
- K220175: GM85 (2022), 3 descendants of its own

## Indications for use
The GF50A Digital X-ray Imaging System is intended for use in generating radiographic images of human anatomy by a qualified/trained doctor or technician. This device is not intended for mammographic applications.

Source page: https://510kreport.com/device/K151419
Methodology: https://510kreport.com/methodology