# K952188: Adviewer 2000

- Pathway: 510(k) (Traditional)
- Applicant: Adp, Ltd.
- Decided: May 30, 1995 after 21 days
- Product code: IXC (Illuminator, Radiographic-Film)
- Device class: 1
- Regulation: 21 CFR 892.1890
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite 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)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K991302: Smartlight Digital Film Viewer, Models SL 4000PLUS, SL 2000PLUS (1999), 0 descendants of its own
- K973965: Smart Motorized Viewer (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K952188
Methodology: https://510kreport.com/methodology