Coeur, Inc. · Class II · Cleared Oct 4, 2007
| K-number | K070798 |
| Device name | ADAPTERS FOR CT, ANGIOGRAPHIC, AND/OR MRI POWER INJECTORS |
| Applicant | Coeur, Inc. |
| Product code | DXT |
| Device class | Class II |
| Decision date | Oct 4, 2007 |
| 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