510(k) K915751 ยท EZN Dilator, Catheter, Ureteral
URETEROMAT 4400
| Applicant | F.M. Wiest USA, Inc., Oradell NJ, US |
| Decision | Substantially Equivalent, Apr 24, 1992 |
| Received | Dec 23, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915751
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.