# K042791: Instant-X, Models 1713 & 128

- Pathway: 510(k) (Traditional)
- Applicant: Ann Arbor Digital Devices
- Decided: Jul 1, 2005 after 267 days
- Product code: MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager))
- 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
This device is called Instant-X and is available as Model 1713 and Model 128. This Device is a digital X-Ray system intended for use in the field of diagnostic X-Ray. The resident physician would use this device just as if it were a film-based system.

Source page: https://510kreport.com/device/K042791
Methodology: https://510kreport.com/methodology