# K904519: Agfa Diagnostic Center (Adc)

- Pathway: 510(k) (Traditional)
- Applicant: Enhanced Imaging Technologies, Inc.
- Decided: Jun 21, 1991 after 261 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
438 later devices descend from it; 2 cite it directly.
1 of 439 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K974597: Adc Compact (Agfa Diagnostic Center) (1998), 436 descendants of its own
- K013138: Adc Compact Plus (2001), 431 descendants of its own
- K022881: Cedara I-Softview (2002), 413 descendants of its own
- K040468: Cedara I-Softview and Cedara I-Readmammo (2004), 255 descendants of its own
- K053301: Cedara I-Response Cedara Pet/CT (2006), 221 descendants of its own

Source page: https://510kreport.com/device/K904519
Methodology: https://510kreport.com/methodology