510(k) K112565 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
NOVAPORT ONE VASCULAR ACCESS CANNULA
| Applicant | Novalung GmbH, Ann Arbor MI, US |
| Decision | Substantially Equivalent, Dec 6, 2011 |
| Received | Sep 2, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112565
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.