510(k) K034050 ยท DTK Filter, Intravascular, Cardiovascular
CORDIS OPTEASE VENA CAVA FILTER, MODELS 466-F220A AND 466-F220B; RETRIEVABLE CATHETER, MODEL 466-C220F
| Applicant | Cordis Corporation, Warren NJ, US |
| Decision | Substantially Equivalent, Mar 22, 2004 |
| Received | Dec 30, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K034050
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 7, 2013 | Cordis Corporation Cordis OPTEASE Retrieval Inferior Vena Cava (IVC) Filter***REF Cat. No.***466F220A and 466F220B***Vena Cava Filter and Introduction Kit***(BRITE TIP Catheter Sheath Introducer and Angiographic Vessel Terminated |
DTK | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.