510(k) K013578 ยท DWE Tubing, Pump, Cardiopulmonary Bypass
PUMP TUBING
| Applicant | Terumo Cardiovascular Systems Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Jan 22, 2002 |
| Received | Oct 29, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013578
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.