# K081925: Snapshot

- Pathway: 510(k) (Traditional)
- Applicant: Instrumentarium Dental, Palodex Group OY
- Decided: Sep 2, 2008 after 57 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
Longest line of descent: 1 generation back to K063837 (2007). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063837: Sigma M, Instrumentarium Dental, Palodex Group OY (2007) Summary page 1.

## Most influential descendants
- K173646: FS Ergo (2017), 0 descendants of its own

## Indications for use
Snapshot is intended to be used by dentists and other qualified professionals for producing diagnostic x-ray radiographs of dentition, jaws and other oral structures.

Source page: https://510kreport.com/device/K081925
Methodology: https://510kreport.com/methodology