Warner-Lambert Co. · Class II · Cleared Nov 21, 1983
| K-number | K833092 |
| Device name | DESERET ANGIO-GUIDE LARGE VEIN CATH. |
| Applicant | Warner-Lambert Co. |
| Product code | FOZ |
| Device class | Class II |
| Decision date | Nov 21, 1983 |
| Decision | Substantially Equivalent |
| Regulation | 880.5200 |
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