Hologic, Inc. · Class II · Cleared Jul 28, 2006
| K-number | K061561 |
| Device name | HIP STRUCTURAL ANALYSIS SOFTWARE OPTION FOR THE HOLOGIC QDR X-RAY BONE DENSITOMETERS |
| Applicant | Hologic, Inc. |
| Product code | KGI |
| Device class | Class II |
| Decision date | Jul 28, 2006 |
| 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