Cordis Corp. · Class II · Cleared Jun 28, 1991
| K-number | K911703 |
| Device name | CORDIS 8 FRENCH 0.084 I.D. PTCA GUIDING CATHETER |
| Applicant | Cordis Corp. |
| Product code | DQO |
| Device class | Class II |
| Decision date | Jun 28, 1991 |
| Decision | Substantially Equivalent |
| Regulation | 870.1200 |
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