# K964263: Expert-KL and Hand Acquisition and Analysis Software

- Pathway: 510(k) (Traditional)
- Applicant: Lunar Corp.
- Decided: Nov 7, 1996 after 13 days
- Product code: KGI (Densitometer, Bone)
- Device class: 2
- Regulation: 21 CFR 892.1170
- 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 K915535 (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)
- K915535: Forearm Software for Lunar DPX Series Bone Desitom, Lunar (1992) Summary page 1.
- K953032: Lunar DPX Densitometer, Lunar Corp. (1995) Summary page 1.

Source page: https://510kreport.com/device/K964263
Methodology: https://510kreport.com/methodology