510(k) K110980 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
CENTRIMAG RETURN CANNULA KIT
| Applicant | Levitronix, LLC, Waltham MA, US |
| Decision | Substantially Equivalent, Jun 20, 2011 |
| Received | Apr 7, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K110980
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.