| K-number | K071250 |
| Device name | CA, MODEL: CAM |
| Applicant | Optovue, Inc. |
| Product code | OBO |
| Device class | Class II |
| Decision date | Sep 28, 2007 |
| Decision | Substantially Equivalent |
| Regulation | 886.1570 |
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