510(k) K883948 ยท DYG Catheter, Flow Directed
MODIFIED NUMED BALLOON ANGIOGRAPHIC CATHETER
| Applicant | NuMED, Inc., Hopkinton NY, US |
| Decision | Substantially Equivalent, Apr 21, 1989 |
| Received | Sep 13, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883948
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.