510(k) K863177 ยท DTL Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
CORDIS ANGIOPLASTY HEMOSTASIS DEVICES
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Oct 15, 1986 |
| Received | Aug 18, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863177
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.