# K072439: GE Lunar DPX & Prodigy Series Dexa Bone Densitometers with Mobile Kit

- Pathway: 510(k) (Special)
- Applicant: Ge Medical Systems Ultrasound and Primary Care Dia
- Decided: Sep 14, 2007 after 15 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: 3 generations back to K890121 (1990). 16 ancestors in all.
No later device cites it as a predicate yet.
0 of 17 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.
- K982267: DPX-RX Bone Densitometer, Lunar Corp. (1998) Summary page 1.
- K983564: Prodigy Total Body Software, Lunar Corp. (1998) Summary page 1.
- K000826: Prodigy Lateral View Software, Lunar Corp. (2000) Summary page 1.
- K001756: Lunar Report Generator II, Lunar Corp. (2000) Summary page 1.
- K001812: Pediatric Reference Data, Lunar Corp. (2000) Summary page 1.
- K011917: Advanced Hip Assessment Software, Ge Lunar Corp. (2001) Summary page 1.
- K023554: Dual-Energy Vertebral Assessment View Software, Ge Lunar Corp. (2002) Summary page 1.

## Indications for use
The GE Lunar DPX and Prodigy Series DEXA Bone Densitometers with Mobile Kit provide a measurement of bone mineral density and fat and lean tissue mass. The values can then be compared to a reference population at the sole discretion of the physician.

Source page: https://510kreport.com/device/K072439
Methodology: https://510kreport.com/methodology