| K-number | K943357 |
| Device name | CEMAX SCANLINK V |
| Applicant | Cemax, Inc. |
| Product code | LMA |
| Device class | Class II |
| Decision date | Nov 22, 1994 |
| Decision | Substantially Equivalent |
| Regulation | 892.2030 |
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