# K873296: DPX Bone Densitometer

- Pathway: 510(k) (Traditional)
- Applicant: Lunar Radiation Corp.
- Decided: Jun 6, 1988 after 294 days
- Product code: KGI (Densitometer, Bone)
- Device class: 2
- Regulation: 21 CFR 892.1170
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Recalls of this device
- Mar 16, 2018 · Class II · Z-1394-2018: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a report for a bone density exam may be sent to PACS with the incorrect patient information in the DICOM header. The correct 

Source page: https://510kreport.com/device/K873296
Methodology: https://510kreport.com/methodology