510(k) K842632 ยท EZN Dilator, Catheter, Ureteral
DILATOR/SHEATH SET
| Applicant | American Edwards Laboratories, Walker MI, US |
| Decision | Substantially Equivalent, Oct 2, 1984 |
| Received | Jul 6, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842632
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.