Carl Zeiss Meditec, Inc. · Class II · Cleared Jan 26, 2007
| K-number | K063378 |
| Device name | CIRRUS HD-OCT, MODEL 4000 |
| Applicant | Carl Zeiss Meditec, Inc. |
| Product code | HLI |
| Device class | Class II |
| Decision date | Jan 26, 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