# K802047: Amx-Iii

- Pathway: 510(k) (Traditional)
- Applicant: General Electric Co.
- Decided: Oct 23, 1980 after 59 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
No predicates in its family tree.
10 later devices descend from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K021016: Amx-4 Plus Mobile X-Ray System (2002), 9 descendants of its own
- K103476: BRIVOXR285AMX, Optima XR200AMX, OPTIMAXR220AMX (2011), 5 descendants of its own
- K142383: Optima XR200amx, Optima XR220amx (2014), 4 descendants of its own
- K162990: Optima XR240amx (2016), 3 descendants of its own
- K173602: Optima XR240amx, AutoGrid (2018), 2 descendants of its own

Source page: https://510kreport.com/device/K802047
Methodology: https://510kreport.com/methodology