# K961944: Lunar Report Generator

- Pathway: 510(k) (Traditional)
- Applicant: Lunar Corp.
- Decided: Jul 3, 1996 after 44 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 K934040 (1994). 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)
- K934040: The Osteoreport, Woodson and Associates, LLC (1994) Summary page 1.

## Indications for use
The LUNAR Report Generator is provided as a software accessory to Lunar Corporation DPX and EXPERT bone mineral densitometers. The Report Generator assists the physician in communicating densitometer results to the patient and the patient’s referring physician.

Source page: https://510kreport.com/device/K961944
Methodology: https://510kreport.com/methodology