# K180663: LaVid FMTS DIAGNOSTIC X-RAY SYSTEM

- Pathway: 510(k) (Traditional)
- Applicant: Livermoretech, Inc.
- Decided: May 18, 2018 after 65 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The LaVid FMTS System is a stationery X-ray system intended for obtaining radiographic images of various portions of the human body, both pediatrics and adults, in a clinical environment. The LaVid FMTS System is not intended for mammography, angiography, interventional, or fluoroscopy use.

Source page: https://510kreport.com/device/K180663
Methodology: https://510kreport.com/methodology