510(k) K030154 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
IDEAL: SYSTEM WITH INTEGRATED VENOUS AIR REMOVAL, CENTRIFUGAL BLOOD PUMP, PUMP BRACKET, ADULT MEMBRANE OXYGENATOR
| Applicant | Dideco S.P.A., Waltham MA, US |
| Decision | Substantially Equivalent, Mar 31, 2003 |
| Received | Jan 16, 2003 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K030154
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.