510(k) K050890 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
ECC.O SYSTEM
| Applicant | Dideco S.R.L., Waltham MA, US |
| Decision | Substantially Equivalent, May 5, 2005 |
| Received | Apr 8, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K050890
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.