# K001756: Lunar Report Generator II

- Pathway: 510(k) (Traditional)
- Applicant: Lunar Corp.
- Decided: Jul 6, 2000 after 27 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
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K052581: Lunar Idxa (2005), 1 descendant of its own
- K252718: Lunar Astra (2026), 0 descendants of its own
- K072439: GE Lunar DPX & Prodigy Series Dexa Bone Densitometers with Mobile Kit (2007), 0 descendants of its own

Source page: https://510kreport.com/device/K001756
Methodology: https://510kreport.com/methodology