| K-number | K811172 |
| Device name | VICON |
| Applicant | Oxford Medilog, Inc. |
| Product code | LXJ |
| Device class | Class II |
| Decision date | Jun 16, 1981 |
| Decision | Substantially Equivalent |
| Regulation | 890.5360 |
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