Guidant Corp. · Class II · Cleared Jan 27, 2000
| K-number | K993639 |
| Device name | RX VIATRAC 18 PERIPHERAL DILATATION CATHETER, OTW VIATRAC 18 PERIPHERAL DILATATION CATHETER |
| Applicant | Guidant Corp. |
| Product code | LIT |
| Device class | Class II |
| Decision date | Jan 27, 2000 |
| Decision | Substantially Equivalent |
| Regulation | 870.1250 |
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