# K053558: Ceph, Model 4900

- Pathway: 510(k) (Traditional)
- Applicant: Schick Technologies, Inc.
- Decided: Feb 17, 2006 after 58 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: 2 generations back to K933455 (1994). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K837506: Kodak T-Mat G Film SO-381, Eastman Kodak Company (1983) Summary page 1.
- K031291: CDR Panx, Model 4792, Schick Technologies, Inc. (2003) Summary page 1.
- K041385: Modification to Computed Oral Radiology System, Schick Technologies, Inc. (2004) Summary page 1.

## Indications for use
The Ceph Model 4900 is indicated for individuals requiring extra-oral dental examinations.

Source page: https://510kreport.com/device/K053558
Methodology: https://510kreport.com/methodology
