510(k) K940542 ยท EZN Dilator, Catheter, Ureteral
NAMIC ARIA(TM) INFLATION DEVICE
| Applicant | American Medical Systems, Inc., Minnetonka MN, US |
| Decision | Substantially Equivalent, Apr 18, 1994 |
| Received | Feb 7, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K940542
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.