Medrad, Inc. · Class II · Cleared Dec 10, 2004
| K-number | K042784 |
| Device name | MEDRAD SPECTRIS SOLARIS EP MR INJECTOR SYSTEM |
| Applicant | Medrad, Inc. |
| Product code | DXT |
| Device class | Class II |
| Decision date | Dec 10, 2004 |
| Decision | Substantially Equivalent |
| Regulation | 870.1650 |
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