# K973965: Smart Motorized Viewer

- Pathway: 510(k) (Traditional)
- Applicant: Smartlight, Ltd.
- Decided: Dec 12, 1997 after 56 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
Longest line of descent: 1 generation back to K922079 (1992). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K922079: Rotolux, Selectolux, Shuttervue, American Medical Sales, Inc. (1992) Summary page 1.
- K952188: Adviewer 2000, Adp, Ltd. (1995) Summary page 1.
- (no number) S&S/Radx MV220/MV400: named in the summary without a submission number

## Indications for use
Radiographic Film Reading

Source page: https://510kreport.com/device/K973965
Methodology: https://510kreport.com/methodology