# K013893: SCANX

- Pathway: 510(k) (Traditional)
- Applicant: Air Techniques, Inc.
- Decided: Feb 1, 2002 after 70 days
- Product code: MUH (System, X-Ray, Extraoral Source, Digital)
- Device class: 2
- Regulation: 21 CFR 872.1800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices 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.

## Most influential descendants
- K101289: Scanx D5000 Series Scanner Model: D5000-F, D5000-FB, D5000-FVB, D5000-Q, D5000-QB (2010), 0 descendants of its own

## Indications for use
The ScanX Scanner is a device that scans photostimulable phosphor plates that have been exposed in the place of dental x-ray film and allows those images to be displayed on a CRT and stored for later recovery in a computer memory. it will be used by dentists and authorized dental auxiliary personnel for this purpose.

Source page: https://510kreport.com/device/K013893
Methodology: https://510kreport.com/methodology