| K-number | K972484 |
| Device name | ACS VIKING GUIDING CATHETER |
| Applicant | Guidant Corp. |
| Product code | DQY |
| Device class | Class II |
| Decision date | Sep 26, 1997 |
| 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