Hologic, Inc. · Class II · Cleared Nov 8, 2002
| K-number | K023398 |
| Device name | HOLOGIC QDR X-RAY BONE DENSITOMETER, MODELS 1000, 2000, 4500, DELPHI, DISCOVERY |
| Applicant | Hologic, Inc. |
| Product code | KGI |
| Device class | Class II |
| Decision date | Nov 8, 2002 |
| 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