510(k) K003902 ยท DQO Catheter, Intravascular, Diagnostic
MULTITRACK ANGIOGRAPHIC CATHETER
| Applicant | NuMED, Inc., Nicholville NY, US |
| Decision | Substantially Equivalent, Jan 11, 2001 |
| Received | Dec 19, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K003902
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.