510(k) K081680 ยท DQY Catheter, Percutaneous
NUCLEUS-X, MODEL 230X
| Applicant | NuMED, Inc., Hopkinton NY, US |
| Decision | Substantially Equivalent, Jul 10, 2008 |
| Received | Jun 17, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K081680
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.