AGILTRAC .018 PERIPHERAL DILATATION CATHETER — Guidant Corp. (510(k) K020161)
AGILTRAC .018 PERIPHERAL DILATATION CATHETER — Guidant Corp. (510(k) K020161) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: AGILTRAC .018 PERIPHERAL DILATATION CATHETER; Applicant: Guidant Corp.; Clearance track: 510(k).
| Device name | AGILTRAC .018 PERIPHERAL DILATATION CATHETER |
|---|---|
| Applicant | Guidant Corp. |
| Clearance track | 510(k) |
| Submission number | K020161 |
| Decision | Substantially Equivalent |
| Decision date | 2002-02-22 |
| Date received | 2002-01-17 |
| Product code | DQY |
| Device class | 2 |
| Medical specialty | Cardiovascular |
| Applicant location | CA, US |
| Source | openFDA device |
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