510(k) K831189 ยท DQO Catheter, Intravascular, Diagnostic
ANGIOGRAPHIC NEEDLE
| Applicant | Medrad, Inc., Walker MI, US |
| Decision | Substantially Equivalent, May 9, 1983 |
| Received | Apr 12, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831189
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.