Hologic, Inc. · Class II · Cleared Jun 13, 1997
| K-number | K961787 |
| Device name | BODY COMPOSITION SOFTWARE OPTION FOR QDR X-RAY BONE DENSITOMETERS |
| Applicant | Hologic, Inc. |
| Product code | KGI |
| Device class | Class II |
| Decision date | Jun 13, 1997 |
| 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