# K031291: CDR Panx, Model 4792

- Pathway: 510(k) (Traditional)
- Applicant: Schick Technologies, Inc.
- Decided: May 5, 2003 after 12 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. The FDA summary names its predicate without a number.
- (no number) Soredex Cranex Tome system: named in the summary without a submission number

## Most influential descendants
- K053558: Ceph, Model 4900 (2006), 0 descendants of its own

## Indications for use
The CDR PanX Model 4792 is indicated for individuals requiring extra-oral dental exams. It exposes and acquires radiographic images at the dento-maxillofacial region.

Source page: https://510kreport.com/device/K031291
Methodology: https://510kreport.com/methodology
