Hologic, Inc. · Class II · Cleared Oct 1, 1999
| K-number | K992775 |
| Device name | OPTION FOR THE QDR BONE DENSITOMETER, MODELS QDR4500, QDR2000, QDR1500, QDR4000, QDR1000, QDR1000W |
| Applicant | Hologic, Inc. |
| Product code | KGI |
| Device class | Class II |
| Decision date | Oct 1, 1999 |
| 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