510(k) K023116 ยท DTK Filter, Intravascular, Cardiovascular
CORDIS OPTEASE PERMANENT VENA CAVA FILTER, MODELS 466-F200A, 466-F200B
| Applicant | Cordis Corp., Warren NJ, US |
| Decision | Unknown, Oct 18, 2002 |
| Received | Sep 19, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K023116
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.