# K980722: Trimax Radiographic Cassette

- Pathway: 510(k) (Traditional)
- Applicant: Imation Corp.
- Decided: Mar 23, 1998 after 27 days
- Product code: IXA (Cassette, Radiographic Film)
- Device class: 2
- Regulation: 21 CFR 892.1850
- 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. The FDA summary names its predicate without a number.
- (no number) DuPont/Sterling Intensifying Screens and Cassettes: named in the summary without a submission number

## Most influential descendants
- K081557: Portable Supine Patient Support and Cassette Holder (2008), 0 descendants of its own
- K012373: Liferay WL Cassette, Liferay KW Cassette (2001), 0 descendants of its own

## Indications for use
Imation Trimax Cassettes are intended for use during diagnostic x-ray procedures to hold a radiographic film in close contact with an x-ray intensifying screen and to provide a light-proof enclosure for direct exposure of radiographic film.

Source page: https://510kreport.com/device/K980722
Methodology: https://510kreport.com/methodology