| K-number | K903923 |
| Device name | USCI(R) SILK (TM) GUIDE WIRE |
| Applicant | C.R. Bard, Inc. |
| Product code | DQX |
| Device class | Class II |
| Decision date | Nov 21, 1990 |
| Decision | Substantially Equivalent |
| Regulation | 870.1330 |
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