Lunar Corp. · Class II · Cleared Nov 18, 1998
| K-number | K983269 |
| Device name | FRACTURE RISK ASSESSMENT OPTION FOR EXPERT-XL BONE DENSITOMETER |
| Applicant | Lunar Corp. |
| Product code | KGI |
| Device class | Class II |
| Decision date | Nov 18, 1998 |
| Decision | Substantially Equivalent |
| Regulation | 892.1170 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov