Imris, Inc. · Class II · Cleared Mar 23, 2012
| K-number | K113748 |
| Device name | IMRIS MR/X-RAY HEAD FIXATION DEVICE (HFD) |
| Applicant | Imris, Inc. |
| Product code | HBL |
| Device class | Class II |
| Decision date | Mar 23, 2012 |
| Decision | Substantially Equivalent |
| Regulation | 882.4460 |
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