# K021542: Adc Dental

- Pathway: 510(k) (Traditional)
- Applicant: Agfa Corp.
- Decided: Aug 6, 2002 after 88 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: 3 generations back to K904519 (1991). 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)
- K013138: Adc Compact Plus, Agfa-Gevaert AG (2001)
- K982661: CDR - Pan  Model 4700, Schick Technologies, Inc. (1998) Summary page 1.

## Indications for use
The ADC Dental is indicated for use to provide diagnostic quality images to aid in physician or dentist diagnosis. The ADC Dental is intended to be used in extraoral dental and maxillofacial imaging applications.

Source page: https://510kreport.com/device/K021542
Methodology: https://510kreport.com/methodology