# K013229: Liferay FW Mammo Cassette, Liferay KW Mammo Casette

- Pathway: 510(k) (Traditional)
- Applicant: Ferrania USA, Inc.
- Decided: Oct 12, 2001 after 15 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
Longest line of descent: 1 generation back to K890361 (1989). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K890361: Kodak Min-R 2 Cassette, Eastman Kodak Company (1989) Summary page 1.

## Indications for use
Ferrania LifeRay™ Mammo Cassettes are intended for use during mammography diagnostic procedures to provide a light-proof enclosure for direct exposure of X-ray films and to hold the film in close contact with an X-ray intensifying screen.

Source page: https://510kreport.com/device/K013229
Methodology: https://510kreport.com/methodology