Guidant Corp. · Class II · Cleared Feb 22, 2002
| K-number | K020161 |
| Device name | AGILTRAC .018 PERIPHERAL DILATATION CATHETER |
| Applicant | Guidant Corp. |
| Product code | DQY |
| Device class | Class II |
| Decision date | Feb 22, 2002 |
| 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