International Regulatory Consultants · Class II · Cleared Oct 9, 1998
| K-number | K981591 |
| Device name | VORTEK URETERAL DOUBLE LOOP STENT, BIOSOFT URETERAL DOUBLE LOOP STENT |
| Applicant | International Regulatory Consultants |
| Product code | FAD |
| Device class | Class II |
| Decision date | Oct 9, 1998 |
| Decision | Substantially Equivalent |
| Regulation | 876.4620 |
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