# K033202: Advantage Paddle

- Pathway: 510(k) (Abbreviated)
- Applicant: Livingston Products, Inc.
- Decided: Dec 3, 2003 after 62 days
- Product code: IZH (System, X-Ray, Mammographic)
- Device class: 2
- Regulation: 21 CFR 892.1710
- 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 K023229 (2002). 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)
- K023229: S.O.F.T. Paddle (Special Optimized Full Compression Tray), Model SFT-Pdle, American Mammographics, Inc. (2002) Summary page 1.

## Indications for use
For use in Screening Mammographic Imaging as a Specialty Paddle for Full Breast Compression as an alternative to conventional breast compression paddles.

Source page: https://510kreport.com/device/K033202
Methodology: https://510kreport.com/methodology