510(k) K854975 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
ELECATH PULSATILE PERFUSION PUMP
| Applicant | Electro-Catheter Corp., Rahway NJ, US |
| Decision | Substantially Equivalent, Jan 15, 1986 |
| Received | Dec 12, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854975
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.