510(k) K140286 ยท DTK Filter, Intravascular, Cardiovascular
OPTEASE VENA CAVA FILTER AND OPTEASE RETRIEVAL CATHTETER
| Applicant | Cordis, A Johnson & Johnson Co., Fremont CA, US |
| Decision | Substantially Equivalent, Mar 7, 2014 |
| Received | Feb 5, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K140286
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.