510(k) K993818 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
ANTEGRADE/RETROGRADE PERFUSION ADAPTER WITH OR WITHOUT PRESSURE LINE
| Applicant | California Medical Laboratories, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Feb 8, 2000 |
| Received | Nov 10, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993818
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.