510(k) K082868 ยท DQY Catheter, Percutaneous
MULLINS-X, MODEL 250X
| Applicant | NuMED, Inc., Hopkinton NY, US |
| Decision | Substantially Equivalent, Oct 24, 2008 |
| Received | Sep 29, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K082868
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.