| K-number | K981819 |
| Device name | ANGIOLAZ VES-1CAM |
| Applicant | Angiolaz, Inc. |
| Product code | FWF |
| Device class | Class I |
| Decision date | Aug 4, 1998 |
| Decision | Substantially Equivalent |
| Regulation | 878.4160 |
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